A Novel Hybrid CFHR1/CFH Gene Causes Atypical Hemolytic Uremic Syndrome

BACKGROUND: Mutations in complement factor H (CFH) are associated with complement dysregulation and the development of an aggressive form of atypical hemolytic uremic syndrome (aHUS) that progresses to end-stage renal disease and in most patients has a high rate of recurrence following transplantati...

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Bibliografiska uppgifter
I publikationen:Pediatr Nephrol
Huvudupphovsmän: Eyler, Stephen J., Meyer, Nicole C., Zhang, Yuzhou, Xiao, Xue, Nester, Carla M., Smith, Richard J.H.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2013
Ämnen:
Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4433496/
https://ncbi.nlm.nih.gov/pubmed/23880784
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-013-2560-2
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