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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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Bibliographic Details
Published in:Blood
Main Author: Afshar-Kharghan, Vahid
Format: Artigo
Language:Inglês
Published: American Society of Hematology 2021
Subjects:
Online Access: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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