The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulation
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Immunology
Reference32 articles.
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2. Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome;Caprioli;Blood,2006
3. Decay accelerating factor (CD55) deficiency phenotypes in Japanese;Daniels;Transfus Med,1998
4. A possible null phenotype in the Cromer blood group complex;Daniels;Transfusion,1982
5. Heterozygous and homozygous Factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases;Dragon-Durey;J. Am. Soc. Nephrol.,2004
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