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Mutations on the Protein: NP_005563 From Positions: 372 To 400

3
0
0
3



OMIM Disease: 150330.0043
p.ARG399CYS
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2


OMIM Disease: 150330.0017
p.ARG377HIS
N/A
N/A
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B||CARDIOMYOPATHY, DILATED, 1A, INCLUDED


OMIM Disease: 150330.0047
p.LEU380SER
N/A
N/A
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED






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