Demir, T. Et Al. 2016. 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. DIABETIC MEDICINE , vol.33, no.10 , 1445-1450.

Demir, T., ONAY, H., Savage, D. B., Temeloglu, E., Uzum, A. K., Kadioglu, P., ... Altay, C.(2016). 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. DIABETIC MEDICINE , vol.33, no.10, 1445-1450.

Demir, T. Et Al. "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," DIABETIC MEDICINE , vol.33, no.10, 1445-1450, 2016

Demir, T. Et Al. "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." DIABETIC MEDICINE , vol.33, no.10, pp.1445-1450, 2016

Demir, T. Et Al. (2016) . "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." DIABETIC MEDICINE , vol.33, no.10, pp.1445-1450.

@article{article, author={T. Demir Et Al. }, title={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}, journal={DIABETIC MEDICINE}, year=2016, pages={1445-1450} }