Whole-exome sequencing with targeted analysis and epilepsy after acute symptomatic neonatal seizures
Abstract
Background The contribution of pathogenic gene variants with development of epilepsy after acute symptomatic neonatal seizures is not known. Methods Case–control study of 20 trios in children with a history of acute symptomatic neonatal seizures: 10 with and 10 without post-neonatal epilepsy. We performed whole-exome sequencing (WES) and identified pathogenic de novo, transmitted, and non-transmitted variants from established and candidate...
Paper Details
Title
Whole-exome sequencing with targeted analysis and epilepsy after acute symptomatic neonatal seizures
Published Date
Apr 12, 2021
Journal
Volume
91
Issue
4
Pages
896 - 902
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