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Mutations on the Protein: O75251 From Positions: 117 To 128

2
1
0
1





Swiss-Prot Disease: VAR_008848
p.VAL122MET
N/A
N/A
Mitochondrial complex I deficiency (MT-C1D)


OMIM Disease: 601825.0001
p.VAL122MET
N/A
N/A
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY






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