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Gain-of-function factor H–related 5 protein impairs glomerular complement regulation resulting in kidney damage
Genetic variation within the factor H–related (FHR) genes is associated with the complement-mediated kidney disease, C3 glomerulopathy (C3G). There is no definitive treatment for C3G, and a significant proportion of patients develop end-stage renal disease. The prototypical example is CFHR5 nephropa...
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| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8020653/ https://ncbi.nlm.nih.gov/pubmed/33753502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.2022722118 |
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