Cargando…

Novel Therapies for Alport Syndrome

Alport syndrome (AS) is a hereditary kidney disease associated with proteinuria, hematuria and progressive kidney failure. It is characterized by a defective glomerular basement membrane caused by mutations in type IV collagen genes COL4A3/A4/A5 which result in defective type IV collagen α3, α4, or...

Descripción completa

Detalles Bibliográficos
Autores principales: Chavez, Efren, Rodriguez, Juanly, Drexler, Yelena, Fornoni, Alessia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081811/
https://www.ncbi.nlm.nih.gov/pubmed/35547199
http://dx.doi.org/10.3389/fmed.2022.848389