Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group-Reference-Cited by-同舟云学术

Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group

Published:2004-12-23 Issue:3 Volume:20 Page:545-551
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Frasca G. M.,Onetti-Muda A.,Mari F.,Longo I.,Scala E.,Pescucci C.,Roccatello D.,Alpa M.,Coppo R.,Volti G. L.,Feriozzi S.,Bergesio F.,Schena F. P.,Renieri A.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/20/3/545/5290783/gfh617.pdf

Reference20 articles.

1. Making the diagnosis of Alport's syndrome

2. Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.

3. Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome

4. Mutations in the COL4A4 gene in thin basement membrane disease

5. Mutations in theCOL4A4andCOL4A3Genes Cause Familial Benign Hematuria

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