The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2007.01867.x/fullpdf
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4. Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*
5. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease
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