PubMed_ArguminSci  

PubMed:27794539 / 125-321 JSONTXT 4 Projects

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Id Subject Object Predicate Lexical cue
T1 0-196 DRI_Approach denotes Mutations in leucine-rich repeat kinase 2 (LRRK2) cause late-onset, autosomal dominant familial Parkinson`s disease (PD) and variation at the LRRK2 locus contributes to the risk for idiopathic PD.