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

Author
ÇALıŞKAN, MİNE
YESIL, Gözde
OZKAN, Melis Ulak
ÖZMEN, Meral
Bektas, Gonca
YILDIZ, Edibe
Metadata
Show full item record
URI
http://hdl.handle.net/20.500.12627/59268
https://doi.org/10.1016/j.seizure.2017.07.011
Collections