Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome
Open Access
- 1 February 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (2), 478-484
- https://doi.org/10.1086/318201
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic SyndromeAmerican Journal of Human Genetics, 2000
- Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic SyndromeAmerican Journal of Human Genetics, 1999
- An integrated map of the human regulator of complement activation (RCA) gene cluster on 1q32Molecular Immunology, 1999
- Genetic studies into inherited and sporadic hemolytic uremic syndromeKidney International, 1998
- Analysis of the recognition mechanism of the alternative pathway of complement by monoclonal anti‐factor H antibodies: evidence for multiple interactions between H and surface bound C3bFEBS Letters, 1996
- Complement factor H and related proteins: an expanding family of complement-regulatory proteins?Immunology Today, 1994
- Human complement factor H: two factor H proteins are derived from alternatively spliced transcriptsEuropean Journal of Immunology, 1991
- Human genes for three complement components that regulate the activation of C3 are tightly linked.The Journal of Experimental Medicine, 1985
- Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution.The Journal of Experimental Medicine, 1977
- Modulation of C3b Hemolytic Activity by a Plasma Protein Distinct from C3b InactivatorScience, 1976