Article
Biomarkers of LRRK2 and lysosomal dysfunction in Progressive Supranuclear Palsy
2025-12-01
Abstract excerpt
<h4>Background</h4> Common and rare genetic variants in LRRK2 have been linked with sporadic and familial Parkinson’s disease (PD). Recently, we discovered that common genetic variation near the LRRK2 locus determined survival in progressive supranuclear palsy (PSP). Our study aimed to explore biomarkers of LRRK2 and lysosomal dysfunction in PSP. <h4>Methods</h4> Immunoblotting was used to measure total LRRK2 an...
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Identifiers and source
- Literature Corpus work
- bad7c43c-f655-5ca8-b526-a245e4e6442b
- DOI
- 10.1101/2025.11.24.25340830
