Whole‐exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci

BACKGROUND: Epilepsy, a serious chronic neurological condition effecting up to 100 million people globally, has clear genetic underpinnings including common and rare variants. In Saudi Arabia, the prevalence of epilepsy is high and caused mainly by perinatal and genetic factors. No whole-exome seque...

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Detalles Bibliográficos
Autores principales: Al Anazi, Abdulrahman H., Ammar, Ahmed S., Al-Hajj, Mahmoud, Cyrus, Cyril, Aljaafari, Danah, Khoda, Iname, Abdelfatah, Ahmed K., Alsulaiman, Abdullah A., Alanazi, Firas, Alanazi, Rawan, Gandla, Divya, Lad, Hetal, Barayan, Samar, Keating, Brendan J., Al-Ali, Amein K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764464/
https://www.ncbi.nlm.nih.gov/pubmed/36539902
http://dx.doi.org/10.1186/s40246-022-00444-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764464/
https://www.ncbi.nlm.nih.gov/pubmed/36539902
http://dx.doi.org/10.1186/s40246-022-00444-6

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