A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene
Gökçen Öz , Serap Teber, Pelin Albayrak, Muhammet Gültekin , Gülhis Deda
(Turk Arch Pediatr 2018; 53: 259-262) DOI: 10.5152/TurkPediatriArs.2018.4197
Gökçen Öz , Serap Teber, Pelin Albayrak, Muhammet Gültekin , Gülhis Deda
(Turk Arch Pediatr 2018; 53: 259-262) DOI: 10.5152/TurkPediatriArs.2018.4197
Burak Tatlı, Ayşe Cebeci, Barış Ekici
(Turk Arch Pediatr 2013; 48: 275-280) DOI: 10.4274/tpa.2083