A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family
Titel:
A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family
Auteur:
Tuncer, Feyza N. Gormez, Zeliha Calik, Mustafa Altiokka Uzun, Gunes Sagiroglu, Mahmut S. Yuceturk, Betul Yuksel, Bayram Baykan, Betul Bebek, Nerses Iscan, Akin Ugur Iseri, Sibel A. Ozbek, Ugur