Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants

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Genome-wide association study reveals genetic risk underlying Parkinson's disease

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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

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Loss of leucine-rich repeat kinase 2 causes impairment of protein degradation pathways, accumulation of α-synuclein, and apoptotic cell death in aged mice

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