Literature DB >> 21563351

Genetics: INF2 mutations often implicated in autosomal dominant focal segmental glomerulosclerosis.

Rebecca Ireland.   

Abstract

Entities:  

Year:  2011        PMID： 21563351     DOI： 10.1038/nrneph.2011.17

Source DB:  PubMed          Journal:  Nat Rev Nephrol        ISSN： 1759-5061            Impact factor:   28.314


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  2 in total

1.  Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.

Authors:  Olivia Boyer; Geneviève Benoit; Olivier Gribouval; Fabien Nevo; Marie-Josèphe Tête; Jacques Dantal; Brigitte Gilbert-Dussardier; Guy Touchard; Alexandre Karras; Claire Presne; Jean-Pierre Grunfeld; Christophe Legendre; Dominique Joly; Philippe Rieu; Nabil Mohsin; Thierry Hannedouche; Valérie Moal; Marie-Claire Gubler; Isabelle Broutin; Géraldine Mollet; Corinne Antignac
Journal:  J Am Soc Nephrol       Date:  2011-01-21       Impact factor: 10.121

2.  Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.

Authors:  Elizabeth J Brown; Johannes S Schlöndorff; Daniel J Becker; Hiroyasu Tsukaguchi; Stephen J Tonna; Andrea L Uscinski; Henry N Higgs; Joel M Henderson; Martin R Pollak
Journal:  Nat Genet       Date:  2009-12-20       Impact factor: 38.330
  2 in total

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