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

Publisher： John Wiley & Sons Inc

E-ISSN： 1464-5491|33|10|1445-1450

ISSN： 0742-3071

Source： DIABETIC MEDICINE, Vol.33, Iss.10, 2016-10, pp. : 1445-1450

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