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Mutations on the Protein: NP_005028 From Positions: 143 To 167

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OMIM Disease: 601487.0015
p.ARG166TRP
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3


OMIM Disease: 601487.0014
p.CYS162SER
N/A
N/A
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3






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