Affiliation:
1. Department of Pathology, University of California, San Diego, San Diego, California, USA
Abstract
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 model for the much more common sporadic PD.
Funder
American Parkinson Disease Association
DOD | United States Army | MEDCOM | Congressionally Directed Medical Research Programs
HHS | NIH | National Institute of Neurological Disorders and Stroke
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
41 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献