Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis-Reference-Cited by-同舟云学术

Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis

Published:2009-12 Issue:12 Volume:76 Page:1268-1276
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Santín Sheila,García-Maset Rafael,Ruíz Patricia,Giménez Isabel,Zamora Isabel,Peña Antonia,Madrid Álvaro,Camacho Juan A.,Fraga Gloria,Sánchez-Moreno Ana,Cobo Maria Ángeles,Bernis Carmen,Ortiz Alberto,de Pablos Augusto Luque,Pintos Guillem,Justa Maria Luisa,Hidalgo-Barquero Emilia,Fernández-Llama Patricia,Ballarín José,Ars Elisabet,Torra Roser,on behalf of the FSGS Spanish Study Group

Publisher

Elsevier BV

Subject

Nephrology

Reference43 articles.

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3. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis;Kaplan;Nat Genet,2000

4. CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility;Kim;Science,2003

5. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis;Winn;Science,2005

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