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...

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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Springer-Verlag 2012
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Original Article
Accés en línia: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
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