| Evidence | Mutation in Nephrotic Syndrome
- Frishberg Y, Rinat C, Megged O, Shapira E, Feinstein S, Raas-Rothschild A, Frishberg Y, Rinat C, Megged O, Shapira E, Feinstein S, Raas-Rothschild A Mutations in NPHS2 encoding podocin are a prevalent cause ofsteroid-resistant nephrotic syndrome among Israeli-Arab children. J Am Soc Nephrol 2002 Feb;13(2):400-5.
Mutation in System Syndrom with Kidney Involvment
Mutation in Nephrosclerosis
- Caridi G, Bertelli R, Carrea A, Di Duca M, Catarsi P, Artero M, Carraro M, Zennaro C, Candiano G, Musante L, Seri M, Ginevri F, Perfumo F, Ghiggeri GM Prevalence, genetics, and clinical features of patients carrying podocinmutations in steroid-resistant nonfamilial focal segmentalglomerulosclerosis. J Am Soc Nephrol 2001 Dec;12(12):2742-6.
Polymorphism in Nephrotic Syndrome
- Narita I, Goto S, Saito N, Song J, Kondo D, Omori K, Kawachi H, Shimizu F, Sakatsume M, Ueno M, Gejyo F Genetic polymorphism of NPHS1 modifies the clinical manifestations of Ig Anephropathy. Lab Invest 2003 Aug;83(8):1193-200.
Other key publications related to this gene
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