A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis

BACKGROUND: Focal segmental glomerulosclerosis (FSGS) is still one of the common causes of refractory nephrotic syndrome. Nephrin, encoded by podocyte-specific NPHS1 gene, participated in the pathogenesis of FSGS. The sites of NPHS1 mutations in FSGS is not clarified very well. In this study, we inv...

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Detalles Bibliográficos
Autores principales: Zhuo, Ling, Huang, Lulin, Yang, Zhenglin, Li, Guisen, Wang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585123/
https://www.ncbi.nlm.nih.gov/pubmed/31216994
http://dx.doi.org/10.1186/s12881-019-0845-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585123/
https://www.ncbi.nlm.nih.gov/pubmed/31216994
http://dx.doi.org/10.1186/s12881-019-0845-4

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