A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene.

A case of Dravet Syndrome with a newly defined mutation in the SCN1A gene. — المؤلف: Tunçer, Gökçen Öz — Turk pediatri arsivi Dec 2018

المؤلف
Tunçer, Gökçen Öz
النشر
Turk pediatri arsivi Dec 2018
الوصف
259-262 p.