Structural and Functional Characterization of Factor H Mutations Associated with Atypical Hemolytic Uremic Syndrome

Author:

Sánchez-Corral Pilar,Pérez-Caballero David,Huarte Olatz,Simckes Ari M.,Goicoechea Elena,López-Trascasa Margarita,de Córdoba Santiago Rodríguez

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference32 articles.

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

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

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

4. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20;Caprioli;J Am Soc Nephrol,2001

5. The role of C4-binding protein and β1H in proteolysis of C4b and C3b;Fujita;J Exp Med,1979

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