Loading...
The Cell Biology of LRRK2 in Parkinson's Disease
Point mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson’s disease (PD) and are implicated in a significant proportion of apparently sporadic PD cases. Clinically, LRRK2-driven PD is indistinguishable from sporadic PD, making it an attractive genetic mo...
Saved in:
| Published in: | Mol Cell Biol |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
American Society for Microbiology
2021
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8088268/ https://ncbi.nlm.nih.gov/pubmed/33526455 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.00660-20 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|