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Mutations on the Protein: O00217 From Positions: 74 To 84

3
1
0
2




Swiss-Prot Disease: VAR_019538
p.PRO79LEU
N/A
N/A
Leigh syndrome (LS)


OMIM Disease: 602141.0005
p.ARG77TRP
N/A
N/A
MITOCHONDRIAL COMPLEX I DEFICIENCY


OMIM Disease: 602141.0001
p.PRO79LEU
N/A
N/A
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY






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