A Rare Cause of Nephrotic Syndrome: The p.Leu364Pro Mutation Associated with Familial Lesitin Cholesterol Acyl Transferase Deficiency

MLA

Nuri Barış Hasbal, et al. “A Rare Cause of Nephrotic Syndrome: The p.Leu364Pro Mutation Associated with Familial Lesitin Cholesterol Acyl Transferase Deficiency.” Turkish Journal of Nephrology, vol. 33, no. 3, July 2024, pp. 303–04. EBSCOhost, https://doi.org/10.5152/turkjnephrol.2024.24782.

APA

Nuri Barış Hasbal, Fatih Palıt, Murat Yaşar Taş, Seyhun Solakoğlu, Işın Kılıçaslan, & Gürsel Yıldız. (2024). A Rare Cause of Nephrotic Syndrome: The p.Leu364Pro Mutation Associated with Familial Lesitin Cholesterol Acyl Transferase Deficiency. Turkish Journal of Nephrology, 33(3), 303–304. https://doi.org/10.5152/turkjnephrol.2024.24782

Chicago

Nuri Barış Hasbal, Fatih Palıt, Murat Yaşar Taş, Seyhun Solakoğlu, Işın Kılıçaslan, and Gürsel Yıldız. 2024. “A Rare Cause of Nephrotic Syndrome: The p.Leu364Pro Mutation Associated with Familial Lesitin Cholesterol Acyl Transferase Deficiency.” Turkish Journal of Nephrology 33 (3): 303–4. doi:10.5152/turkjnephrol.2024.24782.