Novel loss-of-function PRRT2 mutation causes paroxysmal kinesigenic dyskinesia in a Han Chinese...

Background: Mutations in proline-rich transmembrane protein 2 (PRRT2) are a cause of parox http://t.co/ZeBRTgvNi8

via VAT ENGPlus Combo | VATPlus | MotionTrak http://t.co/ZeBRTgvNi8