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...
Gorde:
| Argitaratua izan da: | Blood |
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| Egile nagusia: | |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
American Society of Hematology
2021
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| 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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