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DOAJ Open Access 2024

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

Nuri Barış Hasbal Fatih Palıt Murat Yaşar Taş Seyhun Solakoğlu Işın Kılıçaslan +1 lainnya
Lihat Sumber DOI

Topik & Kata Kunci

Internal medicine Pediatrics

Penulis (6)

N

Nuri Barış Hasbal

F

Fatih Palıt

M

Murat Yaşar Taş

S

Seyhun Solakoğlu

I

Işın Kılıçaslan

G

Gürsel Yıldız

Format Sitasi

APA MLA BibTeX
Hasbal, N.B., Palıt, F., Taş, M.Y., Solakoğlu, S., Kılıçaslan, I., Yıldız, G. (2024). A Rare Cause of Nephrotic Syndrome: The p.Leu364Pro Mutation Associated with Familial Lesitin Cholesterol Acyl Transferase Deficiency. https://doi.org/10.5152/turkjnephrol.2024.24782

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Informasi Jurnal
Tahun Terbit
2024
Sumber Database
DOAJ
DOI
10.5152/turkjnephrol.2024.24782
Akses
Open Access ✓