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Losing control to bad relatives

In this issue of Blood, Martin Merinero et al identified the mechanism of excessive complement activation caused by recurrent mutations in factor H–related protein-1 (FHR-1) in a few patients with atypical hemolytic uremic syndrome (aHUS). These are rare mutations in a rare disease, but the results...

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Detalles Bibliográficos
Publicado en:Blood
Autor Principal: Afshar-Kharghan, Vahid
Formato: Artigo
Idioma:Inglês
Publicado: American Society of Hematology 2021
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8225919/
https://ncbi.nlm.nih.gov/pubmed/34165547
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood.2021011364
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