A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor H

C3 glomerulopathy is a recently described form of CKD. C3GN is a subtype of C3 glomerulopathy characterized by predominant C3 deposits in the glomeruli and is commonly the result of acquired or genetic abnormalities in the alternative pathway (AP) of the complement system. We identified and characte...

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Detalles Bibliográficos
Publicado en:J Am Soc Nephrol
Main Authors: Chauvet, Sophie, Roumenina, Lubka T., Bruneau, Sarah, Marinozzi, Maria Chiara, Rybkine, Tania, Schramm, Elizabeth C., Java, Anuja, Atkinson, John P., Aldigier, Jean Claude, Bridoux, Frank, Touchard, Guy, Fremeaux-Bacchi, Veronique
Formato: Artigo
Idioma:Inglês
Publicado: American Society of Nephrology 2016
Assuntos:
Basic Research
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4884110/
https://ncbi.nlm.nih.gov/pubmed/26471127
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2015040348
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