APA (7th ed.) Citation

Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, & Mehmet Nuri Ozbek. (2023). Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year. Galenos Yayincilik.

Chicago Style (17th ed.) Citation

Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, and Mehmet Nuri Ozbek. Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy Due to Homozygous C.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year. Galenos Yayincilik, 2023.

MLA (9th ed.) Citation

Şervan Özalkak, et al. Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy Due to Homozygous C.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year. Galenos Yayincilik, 2023.