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Mutations on the Protein: P49821 From Positions: 418 To 441

2
1
0
1



Swiss-Prot Disease: VAR_008847
p.THR423MET
N/A
N/A
Leigh syndrome (LS)


OMIM Disease: 161015.0001
p.THR423MET
N/A
N/A
MITOCHONDRIAL COMPLEX I DEFICIENCY






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