Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis-Reference-Cited by-同舟云学术

Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis

Published:2011-01-21 Issue:2 Volume:22 Page:239-245
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Boyer Olivia,Benoit Geneviève,Gribouval Olivier,Nevo Fabien,Tête Marie-Josèphe,Dantal Jacques,Gilbert-Dussardier Brigitte,Touchard Guy,Karras Alexandre,Presne Claire,Grunfeld Jean-Pierre,Legendre Christophe,Joly Dominique,Rieu Philippe,Mohsin Nabil,Hannedouche Thierry,Moal Valérie,Gubler Marie-Claire,Broutin Isabelle,Mollet Géraldine,Antignac Corinne

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference20 articles.

1. Long-term outcome in children and adults with classic focal segmental glomerulosclerosis;Cattran;Am J Kidney Dis,1998

2. Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

3. Mutational and Biological Analysis of α-Actinin-4 in Focal Segmental Glomerulosclerosis

4. A Novel TRPC6 Mutation That Causes Childhood FSGS

5. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

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