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