Unravelling the Role of PAX2 Mutation in Human Focal Segmental Glomerulosclerosis

No effective treatments are available for familial steroid-resistant Focal Segmental Glomerulosclerosis (FSGS), characterized by proteinuria due to ultrastructural abnormalities in glomerular podocytes. Here, we studied a private PAX2 mutation identified in a patient who developed FSGS in adulthood....

Descripción completa

Detalles Bibliográficos
Autores principales: Longaretti, Lorena, Trionfini, Piera, Brizi, Valerio, Xinaris, Christodoulos, Mele, Caterina, Breno, Matteo, Romano, Elena, Giampietro, Roberta, Remuzzi, Giuseppe, Benigni, Ariela, Tomasoni, Susanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698597/
https://www.ncbi.nlm.nih.gov/pubmed/34944624
http://dx.doi.org/10.3390/biomedicines9121808

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698597/
https://www.ncbi.nlm.nih.gov/pubmed/34944624
http://dx.doi.org/10.3390/biomedicines9121808

Ejemplares similares