Expanding the canvas of PRKN mutations in familial and early-onset Parkinson disease.

Expanding the canvas of PRKN mutations in familial and early-onset Parkinson disease.
Related ArticlesExpanding the canvas of PRKN mutations in familial and early-onset Parkinson disease. Parkinsonism Relat Disord. 2019 Aug 09;: Authors: Pandey S, Tomar LR, Kumar S, Dinesh S, Thelma BK Abstract BACKGROUND: Mutations in PRKN (PARK2) are commonly encountered in early-onset Parkinson disease (PD). OBJECTIVES: To screen for PRKN mutations in a clinically well-characterized cohort of early-onset PD patients with ... read more
Source: PubMedPublished on 2019-08-15