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Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -[gamma] (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
Demir, T, Onay, H, Savage, D B, Temeloglu, E, Uzum, A K, Kadioglu, P, Altay, C, Ozen, S, Demir, L, Cavdar, U, Akinci, B
Published in Diabetic medicine (01.10.2016)
Published in Diabetic medicine (01.10.2016)
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