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HARVARD Citation
Demir, T. et al. (n.d.). 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. Diabetic medicine. 33 (10), pp. 1445-1450. [Online].