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Mutations on the Protein: P49638 From Positions: 97 To 111

2
1
0
1




Swiss-Prot Disease: VAR_005668
p.HIS101GLN
N/A
N/A
Ataxia with isolated vitamin E deficiency (AVED)


OMIM Disease: 600415.0002
p.HIS101GLN
N/A
N/A
ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY






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