Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy

ABSTRACT: Atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G) have been linked to mutations in many of the proteins that are involved in alternative complement pathway activation. Age and etiology confounded, the prevalence of such mutations has been reported to be over 30 to 50% i...

Descripción completa

Detalles Bibliográficos
Autores principales: Haydock, Ludwig, Garneau, Alexandre P., Tremblay, Laurence, Yen, Hai-Yun, Gao, Hanlin, Harrisson, Raphaël, Isenring, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770394/
https://www.ncbi.nlm.nih.gov/pubmed/34714369
http://dx.doi.org/10.1007/s00109-021-02102-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770394/
https://www.ncbi.nlm.nih.gov/pubmed/34714369
http://dx.doi.org/10.1007/s00109-021-02102-1

Ejemplares similares