1. 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. Issue 10 (5th February 2016) Authors: Demir, T.; Onay, H.; Savage, D. B.; Temeloglu, E.; Uzum, A. K.; Kadioglu, P.; Altay, C.; Ozen, S.; Demir, L.; Cavdar, U.; Akinci, B. Journal: Diabetic medicine Issue: Volume 33:Issue 10(2016:Oct.) Page Start: 1445 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗