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A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome
Atypical hemolytic uremic syndrome (aHUS) is a complex complement-mediated disease that progresses to end-stage renal failure (ESRF) in 50% of cases. Dysregulation of the alternative pathway (AP) of the complement cascade manifests as microangiopathic anaemia and thrombocytopenia. Multiple genes in...
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| Publicado no: | Nephrol Dial Transplant |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6937010/ https://ncbi.nlm.nih.gov/pubmed/20974643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ndt/gfq658 |
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