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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....

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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

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