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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Argitaratua izan da:Nephrol Dial Transplant
Egile Nagusiak: Maga, Tara K., Meyer, Nicole C., Belsha, Craig, Nishimura, Carla J., Zhang, Yuzhou, Smith, Richard J. H.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2011
Gaiak:
Exceptional Case
Sarrera elektronikoa: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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