Tuncer, F. N. Et Al. 2015. A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family. EPILEPSY RESEARCH , vol.113 , 5-10.

Tuncer, F. N., Görmez, Z., Calik, M., Uzun, G. A., SAGIROGLU, M. S., YUCETURK, B., ... YUKSEL, B.(2015). A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family. EPILEPSY RESEARCH , vol.113, 5-10.

Tuncer, Feyza Et Al. "A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family," EPILEPSY RESEARCH , vol.113, 5-10, 2015

Tuncer, Feyza N. Et Al. "A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family." EPILEPSY RESEARCH , vol.113, pp.5-10, 2015

Tuncer, F. N. Et Al. (2015) . "A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family." EPILEPSY RESEARCH , vol.113, pp.5-10.

@article{article, author={Feyza Nur TUNCER KILINÇ Et Al. }, title={A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family}, journal={EPILEPSY RESEARCH}, year=2015, pages={5-10} }