Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome-Reference-Cited by-同舟云学术

Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome

Published:2005-05-25 Issue:7 Volume:16 Page:2150-2155
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Kavanagh David,Kemp Elizabeth J.,Mayland Elizabeth,Winney Robin J.,Duffield Jeremy S.,Warwick Graham,Richards Anna,Ward Roy,Goodship Judith A,Goodship Timothy H.J.

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference37 articles.

1. The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura

2. Genetic studies into inherited and sporadic hemolytic uremic syndrome

3. Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition

4. The Molecular Basis of Familial Hemolytic Uremic Syndrome: Mutation Analysis of Factor H Gene Reveals a Hot Spot in Short Consensus Repeat 20

5. Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome

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