NPHS2 gene polymorphism aggravates renal damage caused by focal segmental glomerulosclerosis with COL4A3 mutation

Focal segmental glomerulosclerosis (FSGS), a type of primary glomerular disease, is the leading cause of end-stage renal disease (ESRD). Several studies have revealed that certain single-gene mutations are involved in the pathogenesis of FSGS; however, the main cause of FSGS has not been fully eluci...

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Detalles Bibliográficos
Autores principales: Sun, Liping, Zhang, Xinzhou, Wang, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Gastrointestinal, Renal & Hepatic Systems
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786326/
https://www.ncbi.nlm.nih.gov/pubmed/33305316
http://dx.doi.org/10.1042/BSR20203248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7786326/
https://www.ncbi.nlm.nih.gov/pubmed/33305316
http://dx.doi.org/10.1042/BSR20203248

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