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Mutations on the Protein: P25189 From Positions: 186 To 198

2
0
0
2



OMIM Disease: 159440.0036
p.ASP195TYR
N/A
N/A
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B


OMIM Disease: 159440.0013
p.GLN186TER
N/A
N/A
NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT






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