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Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging
DCTN1 mutations in Perry syndrome
Pallidonigral TDP-43 pathology in Perry syndrome
Treatment for the progression of Parkinson's disease
DNAJC13 mutations in Parkinson disease
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
