Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis-Reference-Cited by-同舟云学术

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Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis

Published:2008-06-16 Issue:10 Volume:23 Page:3146-3151
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Lowik M.,Levtchenko E.,Westra D.,Groenen P.,Steenbergen E.,Weening J.,Lilien M.,Monnens L.,Heuvel L. v. d.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/23/10/3146/6901426/gfn208.pdf

Reference25 articles.

1. Circulating Factor Associated with Increased Glomerular Permeability to Albumin in Recurrent Focal Segmental Glomerulosclerosis

2. Genetics of focal segmental glomerulosclerosis

3. Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations

4. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

5. Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

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