A zebrafish model of congenital nephrotic syndrome of the Finnish type

Nephrotic syndrome (NS) is a disease characterized by proteinuria and subsequent hypoalbuminemia, hyperlipidemia and edema due to the defective renal glomerular filtration barrier (GFB). Mutations of NPHS1, encoding NEPHRIN, a podocyte protein essential for normal GFB, cause congenital nephrotic syn...

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Detalles Bibliográficos
Autores principales: Lee, Mi-Sun, Devi, Sulochana, He, John Cijiang, Zhou, Weibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515793/
https://www.ncbi.nlm.nih.gov/pubmed/36187478
http://dx.doi.org/10.3389/fcell.2022.976043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515793/
https://www.ncbi.nlm.nih.gov/pubmed/36187478
http://dx.doi.org/10.3389/fcell.2022.976043

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