Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3.
Okubadejo N; Britton A; Crews C; Akinyemi R; Hardy J; Singleton A; Bras J; Plos One, 2008, vol. 3, issue 10, p e3421, ISSN 19326203. ISBN 19326203.

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