Lanean...

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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Blood
Egile nagusia: Afshar-Kharghan, Vahid
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society of Hematology 2021
Gaiak:
Sarrera elektronikoa: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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