Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS-Reference-Cited by-同舟云学术

Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS

Published:2019-05-01 Issue: Volume:10 Page:
ISSN:1664-3224
Container-title:Frontiers in Immunology
language:
Short-container-title:Front. Immunol.

Author:

Valoti Elisabetta,Alberti Marta,Iatropoulos Paraskevas,Piras Rossella,Mele Caterina,Breno Matteo,Cremaschi Alessandra,Bresin Elena,Donadelli Roberta,Alizzi Silvia,Amoroso Antonio,Benigni Ariela,Remuzzi Giuseppe,Noris Marina

Publisher

Frontiers Media SA

Subject

Immunology,Immunology and Allergy

Reference75 articles.

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4. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome;Richards;Proc Natl Acad Sci USA.,2003

5. Familial haemolytic uraemic syndrome and an MCP mutation;Noris;Lancet.,2003

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