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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Front Genet
Main Authors: Guzzo, Gabriella, Sadallah, Salima, Fodstad, Heidi, Venetz, Jean-Pierre, Rotman, Samuel, Teta, Daniel, Gauthier, Thierry, Pantaleo, Giuseppe, Superti-Furga, Andrea, Pascual, Manuel
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2021
Teme:
Genetics
Online dostop: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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