Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome-Reference-Cited by-同舟云学术

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

Published:2011-08 Issue:4 Volume:80 Page:389-396
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Sanna-Cherchi Simone,Burgess Katelyn E.,Nees Shannon N.,Caridi Gianluca,Weng Patricia L.,Dagnino Monica,Bodria Monica,Carrea Alba,Allegretta Maddalena A.,Kim Hyunjae R.,Perry Brittany J.,Gigante Maddalena,Clark Lorraine N.,Kisselev Sergey,Cusi Daniele,Gesualdo Loreto,Allegri Landino,Scolari Francesco,D'Agati Vivette,Shapiro Lawrence S.,Pecoraro Carmine,Palomero Teresa,Ghiggeri Gian M.,Gharavi Ali G.

Publisher

Elsevier BV

Subject

Nephrology

Reference36 articles.

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3. The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone

4. High incidence of focal segmental glomerulosclerosis in nephrotic syndrome of childhood;Srivastava;Pediatr Nephrol,1999

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

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