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Mutations on the Protein: NP_733822 From Positions: 127 To 159

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OMIM Disease: 150330.0027
p.ARG133LEU
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2||HUTCHINSON-GILFORD PROGERIA SYNDROME, CHILDHOOD-ONSET, INCLUDED


OMIM Disease: 150330.0032
p.ARG133PRO
N/A
N/A
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT


OMIM Disease: 150330.0024
p.GLU145LYS
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL


OMIM Disease: 150330.0031
p.LEU140ARG
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME, CHILDHOOD-ONSET


OMIM Disease: 150330.0034
p.SER143PHE
N/A
N/A
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED






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