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Mutations on the Protein: O43602 From Positions: 44 To 66

3
0
0
3


OMIM Disease: 300121.0005
p.ARG59LEU
N/A
N/A
LISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED


OMIM Disease: 300121.0001
p.ASP62ASN
N/A
N/A
LISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED


OMIM Disease: 300121.0007
p.SER47ARG
N/A
N/A
LISSENCEPHALY, X-LINKED, 1||SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED






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