NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome-Reference-Cited by-同舟云学术

NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome

Published:2007-09-25 Issue:12 Volume:22 Page:2031-2040
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Berdeli Afig,Mir Sevgi,Yavascan Onder,Serdaroglu Erkin,Bak Mustafa,Aksu Nejat,Oner Ayse,Anarat Ali,Donmez Osman,Yildiz Nurhan,Sever Lale,Tabel Yilmaz,Dusunsel Ruhan,Sonmez Ferah,Cakar Nilgun

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-007-0595-y.pdf

Reference36 articles.

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2. International Study of Kidney Disease in Children (1981) 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. Kidney Int 20:765–771

3. Fuchshuber A, Jean G, Gribouval O, Gubler MC, Broyer M, Beckmann JS, Niaudet P, Antignac C (1995) Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis. Hum Mol Genet 4:2155–2158

4. Fuchshuber A, Gribouval O, Ronner V, Kroiss S, Karle S, Brandis M, Hildebrandt F (2001) Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood. J Am Soc Nephrol 12:374–378

5. Kestila M, Lenkkeri U, Mannikko M, Lamerdin J, McCready P, Putaala H, Ruotsalainen V, Morita T, Nissinen M, Herva R, Kashtan CE, Peltonen L, Holmberg C, Olsen A, Tryggvason K (1998) Positionally cloned gene for a novel glomerular protein—nephrin—is mutated in congenital nephrotic syndrome. Mol Cell 4:575–582

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