OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development
Author:
Oner Tulay Oncu,Unalp Aycan,Hiz Semra,Bayram Erhan,Kaytan Ismail,Cingoz Sultan
Publisher
John Libbey Eurotext
Subject
Neurology (clinical),Neurology,General Medicine