Gene: ND2
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Gene: COX1
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Gene: TRNW
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rs199474672 in
ND2;COX1;TRNW gene and
Leigh Disease
PMID 9266739 1997 Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.
PMID 12776230 2003 Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.