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Letter to the Editor

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

Nuri Barış Hasbal 1 , Fatih Palıt 2 , Murat Yaşar Taş 2 , Seyhun Solakoğlu 3 , Işın Kılıçaslan 4 , Gürsel Yıldız 5
1.

Division of Nephrology, Department of Internal Medicine, Koc University School of Medicine, Istanbul, Türkiye

2.

Clinic of Nephrology, Basaksehir Cam and Sakura City Hospital, İstanbul, Türkiye

3.

Department of Histology and Embryology, Istanbul University School of Medicine, İstanbul, Türkiye

4.

Department of Pathology, Istanbul University School of Medicine, İstanbul, Türkiye

5.

Department of Nephrology and Renal Transplantation, Health Sciences University Başakşehir Cam and Sakura Health Application Research Center, İstanbul, Türkiye

Turkish J Nephrol 2024; 33: 303-304
DOI: 10.5152/turkjnephrol.2024.24782
Read: 242 Downloads: 105 Published: 01 July 2024
Volume 33, Issue 3, July 2024
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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.

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