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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...
Autores principales: | Rydberg, Viktor, Aradottir, Sigridur Sunna, Kristoffersson, Ann-Charlotte, Svitacheva, Naila, Karpman, Diana |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
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 |
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