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Mutations on the Protein: O14802 From Positions: 973 To 1043

2
1
0
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Swiss-Prot Disease: VAR_066523
p.ARG1005CYS
N/A
N/A
Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism (HLD7)


OMIM Disease: 614258.0007
p.ARG1005CYS
N/A
N/A
LEUKODYSTROPHY, HYPOMYELINATING, 7, WITHOUT OLIGODONTIA OR HYPOGONADOTROPIC||HYPOGONADISM






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