z-logo
open-access-imgOpen Access
Complement hyperactivation may cause atypical haemolytic uraemic syndrome gain-of-function mutations in factor B
Author(s) -
Jessica Caprioli,
Giuseppe Remuzzi
Publication year - 2007
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfm193
Subject(s) - medicine , atypical hemolytic uremic syndrome , haemolytic uraemic syndrome , hyperactivation , complement system , complement factor b , immunology , alternative complement pathway , complement (music) , mutation , cancer research , genetics , phenotype , antibody , gene , biology , escherichia coli , complementation

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom