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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Detalles Bibliográficos
Autores principales: Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrhman, Rasool, Mahmood, Algahtani, Hussein, Muthaffar, Osama Yousef, Pushparaj, Peter Natesan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257097/
https://www.ncbi.nlm.nih.gov/pubmed/35813387
http://dx.doi.org/10.3389/fped.2022.919996

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257097/
https://www.ncbi.nlm.nih.gov/pubmed/35813387
http://dx.doi.org/10.3389/fped.2022.919996

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