<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE alias="MGO1002" accession="SRS167035">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167035</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205427</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1002</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1002</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1002</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1002</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1002</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503330</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417436</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1004" accession="SRS167037">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167037</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205429</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1004</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1004</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1004</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1004</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1004</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503337</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417443</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1006" accession="SRS167039">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167039</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205431</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1006</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1006</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1006</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1006</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1006</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503303</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417409</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1008" accession="SRS167041">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167041</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205433</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1008</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1008</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1008</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1008</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1008</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503315</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417421</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1010" accession="SRS167043">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167043</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205435</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1010</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1010</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1010</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1010</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1010</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503304</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417410</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1012" accession="SRS167045">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167045</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205437</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1012</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1012</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1012</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1012</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1012</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503280</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417386</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1014" accession="SRS167047">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167047</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205439</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1014</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1014</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1014</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1014</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1014</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503352</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417458</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1016" accession="SRS167049">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167049</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205441</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1016</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1016</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1016</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1016</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1016</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503359</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417465</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1018" accession="SRS167051">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167051</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205443</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1018</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1018</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1018</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1018</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1018</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503318</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417424</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1020" accession="SRS167053">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167053</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205445</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1020</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1020</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fibroblast of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1020</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1020</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1020</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503305</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417411</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fibroblast</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1022" accession="SRS167055">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167055</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205447</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1022</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1022</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1022</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1022</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1022</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503311</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417417</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1024" accession="SRS167057">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167057</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205449</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1024</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1024</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1024</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1024</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1024</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503316</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417422</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1026" accession="SRS167059">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167059</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205451</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1026</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1026</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1026</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1026</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1026</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503291</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417397</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1028" accession="SRS167061">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167061</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205453</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1028</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1028</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1028</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1028</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1028</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503295</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417401</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1030" accession="SRS167063">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167063</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205455</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1030</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1030</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1030</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1030</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1030</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503348</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417454</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1032" accession="SRS167065">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167065</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205457</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1032</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1032</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1032</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1032</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1032</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503329</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417435</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1034" accession="SRS167067">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167067</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205459</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1034</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1034</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1034</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1034</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1034</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503327</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417433</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1036" accession="SRS167069">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167069</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205461</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1036</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1036</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1036</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1036</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1036</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503321</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417427</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1038" accession="SRS167071">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167071</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205463</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1038</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1038</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1038</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1038</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1038</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503283</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417389</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1040" accession="SRS167073">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167073</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205465</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1040</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1040</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1040</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1040</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1040</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503276</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417382</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1042" accession="SRS167075">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167075</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205467</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1042</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1042</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1042</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1042</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1042</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503286</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417392</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1044" accession="SRS167077">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167077</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205469</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1044</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1044</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1044</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1044</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1044</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503299</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417405</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1046" accession="SRS167079">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167079</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205471</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1046</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1046</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1046</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1046</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1046</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503269</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417375</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1048" accession="SRS167081">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167081</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205473</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1048</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1048</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1048</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1048</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1048</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503282</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417388</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1001" accession="SRS167034">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167034</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205426</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1001</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1001</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1001</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1001</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1001</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503323</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417429</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1050" accession="SRS167083">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167083</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205475</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1050</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1050</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1050</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1050</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1050</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503271</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417377</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1003" accession="SRS167036">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167036</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205428</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1003</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1003</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1003</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1003</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1003</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503344</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417450</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1052" accession="SRS167085">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167085</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205477</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1052</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1052</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1052</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1052</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1052</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503331</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417437</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1005" accession="SRS167038">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167038</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205430</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1005</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1005</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1005</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1005</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1005</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503307</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417413</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1054" accession="SRS167087">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167087</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205479</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1054</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1054</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1054</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1054</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1054</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503268</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417374</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1007" accession="SRS167040">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167040</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205432</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1007</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1007</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1007</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1007</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1007</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503360</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417466</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1056" accession="SRS167089">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167089</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205481</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1056</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1056</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1056</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1056</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1056</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503342</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417448</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1009" accession="SRS167042">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167042</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205434</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1009</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1009</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1009</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1009</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1009</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503285</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417391</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1058" accession="SRS167091">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167091</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205483</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1058</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1058</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1058</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1058</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1058</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503355</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417461</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1011" accession="SRS167044">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167044</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205436</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1011</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1011</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1011</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1011</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1011</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503322</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417428</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1060" accession="SRS167093">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167093</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205485</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1060</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1060</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1060</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1060</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1060</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503290</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417396</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1013" accession="SRS167046">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167046</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205438</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1013</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1013</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1013</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1013</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1013</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503349</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417455</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1062" accession="SRS167095">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167095</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205487</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1062</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1062</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1062</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1062</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1062</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503317</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417423</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1015" accession="SRS167048">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167048</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205440</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1015</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1015</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1015</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1015</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1015</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503284</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417390</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1064" accession="SRS167097">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167097</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205489</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1064</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1064</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1064</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1064</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1064</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503357</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417463</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1017" accession="SRS167050">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167050</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205442</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1017</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1017</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1017</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1017</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1017</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503294</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417400</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1066" accession="SRS167099">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167099</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205491</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1066</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1066</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1066</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1066</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1066</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503358</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417464</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1021" accession="SRS167054">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167054</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205446</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1021</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1021</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1021</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1021</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1021</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503264</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417370</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1068" accession="SRS167101">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167101</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205493</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1068</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1068</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1068</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1068</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1068</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503288</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417394</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1023" accession="SRS167056">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167056</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205448</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1023</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1023</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1023</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1023</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1023</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503343</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417449</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1070" accession="SRS167103">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167103</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205495</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1070</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1070</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1070</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1070</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1070</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503336</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417442</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1025" accession="SRS167058">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167058</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205450</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1025</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1025</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1025</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1025</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1025</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503354</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417460</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1072" accession="SRS167105">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167105</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205497</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1072</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1072</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1072</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1072</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1072</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503287</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417393</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1027" accession="SRS167060">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167060</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205452</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1027</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1027</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1027</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1027</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1027</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503302</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417408</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1074" accession="SRS167107">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167107</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205499</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1074</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1074</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1074</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1074</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1074</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503334</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417440</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1029" accession="SRS167062">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167062</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205454</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1029</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1029</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1029</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1029</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1029</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503312</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417418</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1077" accession="SRS167109">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167109</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205501</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1077</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1077</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1077</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1077</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1077</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503346</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417452</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1031" accession="SRS167064">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167064</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205456</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1031</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1031</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1031</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1031</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1031</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503324</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417430</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1079" accession="SRS167111">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167111</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205503</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1079</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1079</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1079</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1079</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1079</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503289</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417395</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1033" accession="SRS167066">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167066</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205458</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1033</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1033</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1033</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1033</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1033</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503325</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417431</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1081" accession="SRS167113">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167113</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205505</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1081</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1081</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1081</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1081</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1081</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503277</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417383</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1035" accession="SRS167068">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167068</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205460</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1035</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1035</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1035</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1035</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1035</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503272</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417378</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1083" accession="SRS167115">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167115</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205507</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1083</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1083</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fibroblast of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1083</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1083</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1083</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503333</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417439</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fibroblast</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1037" accession="SRS167070">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167070</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205462</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1037</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1037</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1037</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1037</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1037</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503267</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417373</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1085" accession="SRS167117">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167117</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205509</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1085</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1085</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1085</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1085</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1085</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503265</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417371</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1039" accession="SRS167072">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167072</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205464</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1039</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1039</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1039</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1039</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1039</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503341</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417447</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1087" accession="SRS167119">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167119</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205511</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1087</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1087</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1087</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1087</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1087</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503356</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417462</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1041" accession="SRS167074">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167074</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205466</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1041</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1041</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1041</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1041</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1041</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503296</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417402</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1089" accession="SRS167121">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167121</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205513</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1089</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1089</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1089</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1089</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1089</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503274</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417380</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1043" accession="SRS167076">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167076</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205468</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1043</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1043</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1043</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1043</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1043</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503335</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417441</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1091" accession="SRS167123">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167123</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205515</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1091</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1091</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1091</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1091</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1091</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503345</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417451</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1045" accession="SRS167078">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167078</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205470</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1045</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1045</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1045</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1045</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1045</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503278</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417384</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1093" accession="SRS167125">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167125</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205517</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1093</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1093</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1093</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1093</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1093</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503292</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417398</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1047" accession="SRS167080">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167080</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205472</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1047</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1047</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1047</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1047</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1047</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503306</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417412</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1095" accession="SRS167127">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167127</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205519</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1095</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1095</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1095</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1095</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1095</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503340</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417446</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1049" accession="SRS167082">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167082</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205474</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1049</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1049</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1049</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1049</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1049</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503350</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417456</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1097" accession="SRS167129">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167129</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205521</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1097</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1097</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1097</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1097</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1097</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503319</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417425</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1051" accession="SRS167084">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167084</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205476</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1051</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1051</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1051</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1051</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1051</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417445</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1099" accession="SRS167131">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167131</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205523</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1099</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1099</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1099</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1099</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1099</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503308</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417414</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1053" accession="SRS167086">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167086</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205478</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1053</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1053</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1053</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1053</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1053</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503266</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417372</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1055" accession="SRS167088">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167088</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205480</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1055</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1055</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1055</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1055</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1055</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503332</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417438</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1101" accession="SRS287668">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287668</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774097</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1101</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1101</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1101</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1101</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1101</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669175</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541669</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1057" accession="SRS167090">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167090</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205482</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1057</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1057</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1057</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1057</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1057</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503351</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417457</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1103" accession="SRS287670">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287670</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774099</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1103</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1103</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1103</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1103</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1103</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669177</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541671</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1059" accession="SRS167092">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167092</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205484</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1059</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1059</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1059</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1059</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1059</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503353</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417459</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1105" accession="SRS287672">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287672</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774101</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1105</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1105</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1105</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1105</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1105</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669179</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541673</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1061" accession="SRS167094">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167094</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205486</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1061</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1061</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1061</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1061</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1061</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503298</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417404</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1107" accession="SRS287674">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287674</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774103</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1107</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1107</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1107</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1107</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1107</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669181</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541675</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1063" accession="SRS167096">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167096</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205488</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1063</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1063</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1063</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1063</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1063</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503275</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417381</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1109" accession="SRS287676">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287676</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774105</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1109</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1109</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1109</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1109</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1109</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669183</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541677</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1065" accession="SRS167098">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167098</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205490</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1065</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1065</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1065</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1065</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1065</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503301</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417407</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1111" accession="SRS287678">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287678</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774107</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1111</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1111</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1111</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1111</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1111</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669185</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541679</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1019" accession="SRS167052">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167052</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205444</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1019</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1019</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1019</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1019</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1019</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503270</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417376</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1113" accession="SRS287680">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287680</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774109</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1113</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1113</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1113</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1113</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1113</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669187</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541681</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1069" accession="SRS167102">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167102</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205494</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1069</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1069</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1069</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1069</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1069</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503328</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417434</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1115" accession="SRS287682">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287682</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774111</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1115</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1115</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1115</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1115</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1115</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669189</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541683</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1071" accession="SRS167104">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167104</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205496</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1071</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1071</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1071</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1071</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1071</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503281</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417387</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1117" accession="SRS287684">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287684</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774113</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1117</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1117</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1117</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1117</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1117</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669191</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541685</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1073" accession="SRS167106">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167106</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205498</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1073</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1073</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1073</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1073</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1073</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503320</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417426</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1119" accession="SRS287686">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287686</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774115</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1119</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1119</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1119</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1119</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1119</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669193</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541687</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1075" accession="SRS167108">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167108</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205500</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1075</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1075</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1075</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1075</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1075</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503263</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417369</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1121" accession="SRS287688">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287688</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774117</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1121</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1121</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1121</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1121</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1121</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669195</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541689</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1078" accession="SRS167110">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167110</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205502</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1078</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1078</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1078</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1078</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1078</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503326</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417432</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1123" accession="SRS287690">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287690</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774119</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1123</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1123</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1123</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1123</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1123</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669197</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541691</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1080" accession="SRS167112">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167112</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205504</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1080</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1080</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1080</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1080</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1080</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503262</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417368</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1125" accession="SRS287692">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287692</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774121</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1125</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1125</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1125</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1125</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1125</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669199</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541693</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1127" accession="SRS287694">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287694</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774123</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1127</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1127</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1127</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1127</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1127</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669201</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541695</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1084" accession="SRS167116">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167116</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205508</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1084</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1084</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1084</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1084</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1084</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503297</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417403</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1129" accession="SRS287696">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287696</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774125</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1129</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1129</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1129</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1129</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1129</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669203</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541697</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1086" accession="SRS167118">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167118</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205510</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1086</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1086</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1086</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1086</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1086</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503273</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417379</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1131" accession="SRS287698">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287698</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774127</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1131</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1131</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1131</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1131</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1131</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669205</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541699</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1088" accession="SRS167120">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167120</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205512</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1088</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1088</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1088</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1088</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1088</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503313</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417419</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1133" accession="SRS287700">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287700</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774129</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1133</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1133</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1133</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1133</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1133</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669207</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541701</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1090" accession="SRS167122">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167122</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205514</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1090</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1090</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1090</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1090</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1090</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503309</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417415</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1135" accession="SRS287702">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287702</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774131</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1135</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1135</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1135</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1135</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1135</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669209</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541703</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1092" accession="SRS167124">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167124</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205516</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1092</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1092</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Brain tissue of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1092</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1092</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1092</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503338</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417444</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Brain tissue</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1094" accession="SRS167126">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167126</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205518</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1094</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1094</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1094</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1094</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1094</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503347</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417453</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1096" accession="SRS167128">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167128</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205520</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1096</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1096</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1096</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1096</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1096</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503300</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417406</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1098" accession="SRS167130">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167130</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205522</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1098</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1098</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1098</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1098</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1098</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503310</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417416</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1100" accession="SRS167132">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167132</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205524</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1100</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1100</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1100</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1100</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1100</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503279</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417385</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1076" accession="SRS287667">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287667</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774096</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1076</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1076</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1076</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1076</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1076</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669174</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541668</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1102" accession="SRS287669">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287669</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774098</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1102</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1102</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1102</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1102</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1102</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669176</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541670</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1104" accession="SRS287671">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287671</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774100</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1104</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1104</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1104</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1104</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1104</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669178</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541672</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1106" accession="SRS287673">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287673</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774102</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1106</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1106</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1106</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1106</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1106</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669180</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541674</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1108" accession="SRS287675">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287675</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774104</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1108</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1108</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1108</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1108</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1108</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669182</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541676</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1110" accession="SRS287677">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287677</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774106</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1110</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1110</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1110</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1110</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1110</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669184</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541678</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1112" accession="SRS287679">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287679</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774108</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1112</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1112</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1112</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1112</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1112</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669186</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541680</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1067" accession="SRS167100">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS167100</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00205492</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1067</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1067</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1067</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1067</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1067</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>503314</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>417420</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1116" accession="SRS287683">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287683</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774112</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1116</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1116</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1116</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1116</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1116</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669190</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541684</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1118" accession="SRS287685">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287685</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774114</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1118</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1118</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1118</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1118</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1118</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669192</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541686</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1120" accession="SRS287687">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287687</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774116</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1120</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1120</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1120</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1120</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1120</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669194</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541688</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1122" accession="SRS287689">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287689</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774118</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1122</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1122</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1122</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1122</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1122</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669196</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541690</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1124" accession="SRS287691">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287691</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774120</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1124</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1124</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Lymphoblastoid cell line of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1124</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1124</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1124</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669198</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541692</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Lymphoblastoid cell line</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1126" accession="SRS287693">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287693</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774122</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1126</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1126</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1126</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1126</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1126</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669200</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541694</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1128" accession="SRS287695">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287695</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774124</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1128</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1128</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1128</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1128</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1128</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669202</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541696</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1130" accession="SRS287697">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287697</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774126</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1130</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1130</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1130</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1130</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1130</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669204</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541698</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1132" accession="SRS287699">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287699</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774128</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1132</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1132</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1132</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1132</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1132</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669206</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541700</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1134" accession="SRS287701">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287701</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774130</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1134</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1134</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human female participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1134</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1134</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1134</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669208</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541702</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="MGO1114" accession="SRS287681">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS287681</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00774110</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">339-MGO1114</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000339" label="submitted sample id">MGO1114</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>DNA sample from Fresh blood of a human male participant in the dbGaP study "MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000339</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>RespiratoryChainDisease</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>MitoExome Sequencing of Mitochondrial OXPHOS Diseases (MGH)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Case-Control</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>MGO1114</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>MGO1114</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>MGO1114</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>669188</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>541682</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>male</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study disease</TAG>
        <VALUE>Mitochondrial Diseases</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Fresh blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>subject is affected</TAG>
        <VALUE>Yes</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>GRU</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
</SAMPLE_SET>
