Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome-Reference-Cited by-同舟云学术

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome

Published:2004-08 Issue:2 Volume:66 Page:564-570
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Ruf Rainer G.,Schultheiss Michael,Lichtenberger Anne,Karle Stephanie M.,Zalewski Isabella,Mucha Bettina,Everding Anne Schulze,Neuhaus Thomas,Patzer Ludwig,Plank Christian,Haas Johannes P.,Ozaltin Fatih,Imm Anita,Fuchshuber Arno,Bakkaloglu Aysin,Hildebrandt Friedhelm

Publisher

Elsevier BV

Subject

Nephrology

Reference33 articles.

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2. Primary nephrotic syndrome in children. Clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularity. A Report of the International Study of Kidney Disease in Children;Iskdc;Kidney Int,1981

3. Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood;Fuchshuber;J Am Soc Nephrol,2001

4. Positionally cloned gene for a novel glomerular protein—nephrin—is mutated in congenital nephrotic syndrome;Kestila;Mol Cell,1998

5. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome;Boute;Nat Genet,2000

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