A Rare Cause of Nephrotic Syndrome: The p.Leu364Pro Mutation Associated with Familial Lesitin Cholesterol Acyl Transferase Deficiency
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Abstract
Cite this article as: Hasbal NB, Palıt F, Taş MY, Solakoglu S, Kılıçaslan I, Yıldız G. A rare cause of nephrotic syndrome: The p.Leu364Pro mutation associated with familial lesitin cholesterol acyl transferase defciency. Turk J Nephrol. 2024;33(3):303-304.