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Mutations on the Protein: NP_005563 From Positions: 143 To 172

3
0
0
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OMIM Disease: 150330.0024
p.GLU145LYS
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL


OMIM Disease: 150330.0028
p.GLU161LYS
N/A
N/A
CARDIOMYOPATHY, DILATED, 1A


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






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