Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome
- 31 May 2000
- journal article
- other
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (5), 1721-1722
- https://doi.org/10.1086/302877
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic SyndromeAmerican Journal of Human Genetics, 1999
- Disruption of Disulfide Bonds Is Responsible for Impaired Secretion in Human Complement Factor H DeficiencyPublished by Elsevier ,1999
- Genetic studies into inherited and sporadic hemolytic uremic syndromeKidney International, 1998
- Human Factor H DeficiencyJournal of Biological Chemistry, 1997
- Complement factor H and related proteins: an expanding family of complement-regulatory proteins?Immunology Today, 1994
- Disulfide bonds are localized within the short consensus repeat units of complement regulatory proteins: C4b-binding proteinBiochemistry, 1989