A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.


YILDIZ E. , YESIL G. , OZKAN M. U. , Bektas G. , ÇALıŞKAN M., ÖZMEN M.

Seizure, cilt.51, ss.77-79, 2017 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier