Prenatal diagnosis of congenital nephrotic syndrome of the Finnish type in a Chinese family-Reference-Cited by-同舟云学术

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Prenatal diagnosis of congenital nephrotic syndrome of the Finnish type in a Chinese family

Published:2021-07 Issue:4 Volume:60 Page:758-762
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Gu Yuling,Han Bing,Zhu Xiaolan,Chen Youguo

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference19 articles.

1. Glomerular basement membrane antigens in congenital and acquired nephrotic syndrome in childhood;Huttunen;Nephron,1976

2. Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations;Lenkkeri;Am J Hum Genet,1999

3. Positionally cloned gene for a novel glomerular protein-nephrin-is mutated in congenital nephrotic syndrome;Kestilä;Mol Cell,1998

4. A familial childhood-onset relapsing nephrotic syndrome;Kitamura;Kidney Int,2007

5. Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS);Schoeb;Nephrol Dial Transplant,2010

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