MAGI2 Mutations Cause Congenital Nephrotic Syndrome-Reference-Cited by-同舟云学术

MAGI2 Mutations Cause Congenital Nephrotic Syndrome

Published:2016-12-08 Issue:5 Volume:28 Page:1614-1621
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Bierzynska Agnieszka,Soderquest Katrina,Dean Philip,Colby Elizabeth,Rollason Ruth,Jones Caroline,Inward Carol D.,McCarthy Hugh J.,Simpson Michael A.,Lord Graham M.,Williams Maggie,Welsh Gavin I.,Koziell Ania B.,Saleem Moin A.

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference27 articles.

1. Simultaneous Sequencing of 24 Genes Associated with Steroid-Resistant Nephrotic Syndrome

2. A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome

3. Genes and podocytes - new insights into mechanisms of podocytopathy.;Bierzynska;Front Endocrinol (Lausanne),2015

4. Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome

5. Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

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