A descriptive study of NPHS1 and NPHS2 mutations in children with congenital nephrotic syndrome-Reference-Cited by-同舟云学术

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A descriptive study of NPHS1 and NPHS2 mutations in children with congenital nephrotic syndrome

Published:2020-09 Issue: Volume:20 Page:100722
ISSN:2452-0144
Container-title:Gene Reports
language:en
Short-container-title:Gene Reports

Author:

Amr Khalda,El-Bassyouni Hala T.,Rabie Eman,Selim Abeer^ORCID,Zaki Moushira E.,Alazem Eman Abobakr Abd,El-Shaer Shereen,Rady Sahar,Salah Doaa M.

Publisher

Elsevier BV

Subject

Genetics

Reference36 articles.

1. Update on congenital nephrotic syndromes and the contribution of US;Avni;Pediatr. Radiol.,2011

2. NPHS2 mutations;Bakr;Indian J. Pediatr.,2013

3. Interactions between thyroid disorders and kidney disease;Basu;Indian J Endocrinol Metab.,2012

4. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome;Berdeli;Pediatr. Nephrol.,2007

5. NPHS 2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum;Bouchireb;Hum. Mutat.,2014

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital Nephrotic Syndrome With a Novel Presentation in Saudi Arabia;Cureus;2020-09-03

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