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Mutations on the Protein: P49459 From Positions: 23 To 30

2
1
0
1






Swiss-Prot Disease: VAR_066628
p.GLY23ARG
N/A
N/A
Mental retardation, X-linked, syndromic, Nascimento-type (MRXSN)


OMIM Disease: 312180.0002
p.GLY23ARG
N/A
N/A
MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE






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