Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy

Whole-Exome Sequencing Identifies Novel SCN1A and CACNB4 Genes Mutations in the Cohort of Saudi Patients With Epilepsy

Epilepsy is a neurological disorder described as recurrent seizures mild to severe convulsions along with conscious loss. There are many different genetic anomalies or non-genetic conditions that affect the brain and cause epilepsy. The exact cause of epilepsy is unknown so far. In this study, whole...

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Bibliographic Details
Main Authors: Muhammad Imran Naseer, Angham Abdulrhman Abdulkareem, Mahmood Rasool, Hussein Algahtani, Osama Yousef Muthaffar, Peter Natesan Pushparaj
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Pediatrics
Subjects:
Epilepsy
SCN1A
CACNB4
WES
Saudi patients
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2022.919996/full

Internet

https://www.frontiersin.org/articles/10.3389/fped.2022.919996/full

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