RIPK3 Contributes to Lyso-Gb3-Induced Podocyte Death
Fabry disease is a lysosomal storage disease with an X-linked heritage caused by absent or decreased activity of lysosomal enzymes named alpha-galactosidase A (α-gal A). Among the various manifestations of Fabry disease, Fabry nephropathy significantly affects patients’ morbidity and mortality. The...
Na minha lista:
| Principais autores: | , , , , , , , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI AG
2021-01-01
|
| Serier: | Cells |
| Fag: | |
| Online adgang: | https://www.mdpi.com/2073-4409/10/2/245 |
| Tags: |
Ingen Tags, Vær først til at tagge denne postø!
|