Tuncer, G. O. Et Al. 2018. A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.53, no.4 , 259-262.

Tuncer, G. O., TEBER, S., Albayrak, P., Kutluk, M. G., & Deda, G., (2018). A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.53, no.4, 259-262.

Tuncer, Gokcen Et Al. "A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene," TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.53, no.4, 259-262, 2018

Tuncer, Gokcen O. Et Al. "A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene." TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.53, no.4, pp.259-262, 2018

Tuncer, G. O. Et Al. (2018) . "A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene." TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.53, no.4, pp.259-262.

@article{article, author={Gokcen Oz Tuncer Et Al. }, title={A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene}, journal={TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS}, year=2018, pages={259-262} }