Loading...
LRRK2 and the Endolysosomal System in Parkinson’s Disease
Mutations in leucine-rich repeat kinase 2 (LRRK2) cause autosomal dominant familial Parkinson’s disease (PD), with pathogenic mutations enhancing LRRK2 kinase activity. There is a growing body of evidence indicating that LRRK2 contributes to neuronal damage and pathology both in familial and sporadi...
Na minha lista:
| Udgivet i: | J Parkinsons Dis |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
IOS Press
2020
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7677880/ https://ncbi.nlm.nih.gov/pubmed/33044192 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JPD-202138 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|