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

• Main Authors: Muhammad Imran Naseer (Author), Angham Abdulrhman Abdulkareem (Author), Mahmood Rasool (Author), Hussein Algahtani (Author), Osama Yousef Muthaffar (Author), Peter Natesan Pushparaj (Author)
• Format: Book
• Published: Frontiers Media S.A., 2022-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...