Genetic investigation of Nordic patients with complement-mediated kidney diseases

BACKGROUND: Complement 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 popul...

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Detalles Bibliográficos
Autores principales: Rydberg, Viktor, Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Svitacheva, Naila, Karpman, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513385/
https://www.ncbi.nlm.nih.gov/pubmed/37744338
http://dx.doi.org/10.3389/fimmu.2023.1254759

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10513385/
https://www.ncbi.nlm.nih.gov/pubmed/37744338
http://dx.doi.org/10.3389/fimmu.2023.1254759

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