Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome-Reference-Cited by-同舟云学术

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

Published:2006-12-20 Issue:1 Volume:104 Page:240-245
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

de Jorge E. G.,Harris C. L.,Esparza-Gordillo J.,Carreras L.,Arranz E. A.,Garrido C. A.,Lopez-Trascasa M.,Sanchez-Corral P.,Morgan B. P.,de Cordoba S. R.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference32 articles.

1. Thrombotic Microangiopathies

2. Infection by Shiga Toxin-Producing Escherichia coli : An Overview

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

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

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