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

Author:

Richards Anna,Buddles Mark R.,Donne Rosemary L.,Kaplan Bernard S.,Kirk Edwin,Venning Michael C.,Tielemans Christian L.,Goodship Judith A.,Goodship Timothy H.J.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference28 articles.

1. Human factor H deficiency—mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism;Ault;J Biol Chem,1997

2. Identification of a heparin-binding domain in the 7th short consensus repeat of complement factor H-1;Blackmore;J Immunol,1996

3. Identification of the second heparin-binding domain in human complement factor H;Blackmore;J Immunol,1998

4. Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome;Buddles;Am J Hum Genet,2000

5. A radiation hybrid map of complement factor H and factor H-related genes;DiazGuillen;Immunogenetics,1999

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