All individuals with variants in gene TRIT1

6 entries on 1 page. Showing entries 1 - 6.
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AscendingIndividual ID     

ID_report     

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VIP     

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00081477 Pat1 PubMed: Kernohan 2017 - F no United States white - - - - mitochondrial respiratory chain deficiency see paper; ... 2 1 Isabelle Thiffault
00081478 Pat2 PubMed: Kernohan 2017 - F no Canada white - - - - mitochondrial respiratory chain deficiency see paper; ... 2 1 Isabelle Thiffault
00081479 Pat3/4 PubMed: Kernohan 2017 family, affected sister/brother F;M no United States white - - - - mitochondrial respiratory chain deficiency see paper; ... 2 2 Isabelle Thiffault
00081547 - PubMed: Yarham 2014, Journal: Yarham 2014 2-generation family, 2 affected sister/brother, unaffected heterozygous carrier parents F;M yes United Kingdom (Great Britain) Pakistani - - - - ? see paper; ..., encephalopathy (HP:0001298) and myoclonic epilepsy (HP:0002123) due to multiple OXPHOS deficiencies in skeletal muscle 1 2 Johan den Dunnen
00289826 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00430720 - - - - yes Pakistan - - - - - epilepsy - 1 1 Sadaf Naz
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