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Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease.

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author: Nobutaka Hattori  Yoshikuni Mizuno  Peter Henry St George-Hyslop  Anthony Lang  Shigeo Murayama  Hiroyuki Tomiyama  Connie Fernández-Cid Marras  Ekaterina Rogaeva 

Publication date July 28, 2011
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