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Mutations on the Protein: NP_001244303 From Positions: 0 To 29

3
0
0
3



OMIM Disease: 150330.0027
p.ARG21LEU
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2||HUTCHINSON-GILFORD PROGERIA SYNDROME, CHILDHOOD-ONSET, INCLUDED


OMIM Disease: 150330.0032
p.ARG21PRO
N/A
N/A
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT


OMIM Disease: 150330.0031
p.LEU28ARG
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME, CHILDHOOD-ONSET






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