Type IV Collagen Mutations in Familial IgA Nephropathy

Author:

Li Yifu,Groopman Emily E.,D’Agati Vivette,Prakash Sindhuri,Zhang Junying,Mizerska-Wasiak Malgorzata,Caliskan Yasar,Fasel David,Karnib Hussein H.,Bono Luisa,Omran Sadek Al,Sabban Essam Al,Kiryluk Krzysztof,Caridi Gianluca,Ghiggeri Gian Marco,Sanna-Cherchi Simone,Scolari Francesco,Gharavi Ali G.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Nephrology

Reference9 articles.

1. New developments in the genetics, pathogenesis, and therapy of IgA nephropathy;Magistroni;Kidney Int,2015

2. IgA nephropathy;Wyatt;N Engl J Med,2013

3. Thin basement membrane disease in patients with familial IgA nephropathy;Frasca;J Nephrol,2004

4. Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36;Paterson;J Am Soc Nephrol,2007

5. Expert consensus guidelines for the genetic diagnosis of Alport syndrome;Savige;Pediatr Nephrol,2019

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