The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome-Reference-Cited by-同舟云学术

The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome

Published:2015-08 Issue:2 Volume:66 Page:263-273
ISSN:0161-5890
Container-title:Molecular Immunology
language:en
Short-container-title:Molecular Immunology

Author:

Martínez-Barricarte Rubén,Heurich Meike^ORCID,López-Perrote Andrés,Tortajada Agustin,Pinto Sheila,López-Trascasa Margarita,Sánchez-Corral Pilar,Morgan B. Paul,Llorca Oscar,Harris Claire L.,Rodríguez de Córdoba Santiago^ORCID

Publisher

Elsevier BV

Subject

Molecular Biology,Immunology

Reference47 articles.

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3. Structural basis for the stabilization of the complement alternative pathway C3 convertase by properdin;Alcorlo;Proc. Natl. Acad. Sci. U. S. A.,2013

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. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease;Caprioli;Hum. Mol. Genet.,2003

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