LRRK2 Gly2385Arg variant is a risk factor of Parkinson’s disease among Han-Chinese from mainland China
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2007.02052.x/fullpdf
Reference29 articles.
1. Description of Parkinson's Disease as a Clinical Syndrome
2. Parkinson's disease: the genetics of a heterogeneous disorder
3. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease
4. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
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