Genetic investigation of Nordic patients with complement-mediated kidney diseases

Genetic investigation of Nordic patients with complement-mediated kidney diseases

BackgroundComplement activation in atypical hemolytic uremic syndrome (aHUS), C3 glomerulonephropathy (C3G) and immune complex-mediated membranoproliferative glomerulonephritis (IC-MPGN) may be associated with rare genetic variants. Here we describe gene variants in the Swedish and Norwegian populat...

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Bibliographic Details
Main Authors: Viktor Rydberg, Sigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Naila Svitacheva, Diana Karpman
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-09-01
Series:Frontiers in Immunology
Subjects:
complement
atypical hemolytic uremic syndrome
C3 glomerulopathy
membranoproliferative glomerulonephritis
genes
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1254759/full

Internet

https://www.frontiersin.org/articles/10.3389/fimmu.2023.1254759/full

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