Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series

BACKGROUND: Epilepsy is the most common neurological disorder that causes spontaneous, unprovoked, and recurrent seizures. Epilepsy is clinically and genetically heterogeneous with various modes of inheritance. The complexity of epilepsy presents a challenge and identification of the causal genetic...

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Detalles Bibliográficos
Autores principales: Sahli, Maryem, Zrhidri, Abdelali, Elaloui, Siham Chafai, Smaili, Wiam, Lyahyai, Jaber, Oudghiri, Fatima Zohra, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706917/
https://www.ncbi.nlm.nih.gov/pubmed/31439038
http://dx.doi.org/10.1186/s13256-019-2203-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706917/
https://www.ncbi.nlm.nih.gov/pubmed/31439038
http://dx.doi.org/10.1186/s13256-019-2203-8

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