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Case Report: A Rare Truncating Variant of the CFHR5 Gene in IgA Nephropathy
IgA nephropathy (IgAN) is the most common primary glomerulonephritis worldwide. Despite appropriate therapy, 20–40% of affected-patients evolve toward end-stage kidney disease (ESKD). Mesangial IgA deposits are the hallmark of IgAN, and complement deposition (C3) seems to differentiate latent IgA me...
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| Pubblicato in: | Front Genet |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8244589/ https://ncbi.nlm.nih.gov/pubmed/34220921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.529236 |
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