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

Mutations in PRKN (PARK2) are commonly encountered in early-onset Parkinson disease (PD).

Source: Parkinsonism and Related Disorders - August 8, 2019 Category: Neurology Authors: Sanjay Pandey, Laxmikant Ramkumarsingh Tomar, Sumeet Kumar, Shreya Dinesh, B.K. Thelma Tags: Short communication Source Type: research