E. P. YILDIZ Et Al. , "A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.," Seizure , vol.51, pp.77-79, 2017
YILDIZ, E. P. Et Al. 2017. A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.. Seizure , vol.51 , 77-79.
YILDIZ, E. P., YILDIZ, E., YEŞİL, G., YESIL, G., OZKAN, M. U., OZKAN, M. U., ... Bektas, G.(2017). A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.. Seizure , vol.51, 77-79.
YILDIZ, Edibe Et Al. "A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.," Seizure , vol.51, 77-79, 2017
YILDIZ, Edibe P. Et Al. "A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.." Seizure , vol.51, pp.77-79, 2017
YILDIZ, E. P. Et Al. (2017) . "A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.." Seizure , vol.51, pp.77-79.
@article{article, author={Edibe Pembegul YILDIZ Et Al. }, title={A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.}, journal={Seizure}, year=2017, pages={77-79} }