A Novel C3 Mutation Causing Increased Formation of the C3 Convertase in Familial Atypical Hemolytic Uremic Syndrome-Reference-Cited by-同舟云学术

A Novel C3 Mutation Causing Increased Formation of the C3 Convertase in Familial Atypical Hemolytic Uremic Syndrome

Published:2012-01-16 Issue:4 Volume:188 Page:2030-2037
ISSN:0022-1767
Container-title:The Journal of Immunology
language:en
Short-container-title:J.I.

Author:

Sartz Lisa,Olin Anders I,Kristoffersson Ann-Charlotte,Ståhl Anne-lie,Johansson Martin E.,Westman Kerstin,Fremeaux-Bacchi Veronique,Nilsson-Ekdahl Kristina,Karpman Diana

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

Reference31 articles.

1. Atypical Hemolytic–Uremic Syndrome

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

3. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

4. Genetic and Functional Analyses of Membrane Cofactor Protein (CD46) Mutations in Atypical Hemolytic Uremic Syndrome

5. Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

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