Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics

BACKGROUND: Mutations in complement factor H (CFH), factor I (CFI), factor B (CFB), thrombomodulin (THBD), C3 and membrane cofactor protein (MCP), and autoantibodies against factor H (αFH) with or without a homozygous deletion in CFH-related protein 1 and 3 (∆CFHR1/3) predispose development of atypi...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Geerdink, Lianne M., Westra, Dineke, van Wijk, Joanna A. E., Dorresteijn, Eiske M., Lilien, Marc R., Davin, Jean-Claude, Kömhoff, Martin, Van Hoeck, Koen, van der Vlugt, Amerins, van den Heuvel, Lambertus P., van de Kar, Nicole C. A. J.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2012
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3382652/
https://ncbi.nlm.nih.gov/pubmed/22410797
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-012-2131-y
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados