Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations

Published 2016 View Full Article

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Title
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
Authors
Keywords
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Journal
DIABETIC MEDICINE
Volume 33, Issue 10, Pages 1445-1450
Publisher
Wiley
Online
2016-01-12
DOI
10.1111/dme.13061
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