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

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

Abstract 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...

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Bibliographic Details
Main Authors: Maryem Sahli, Abdelali Zrhidri, Siham Chafai Elaloui, Wiam Smaili, Jaber Lyahyai, Fatima Zohra Oudghiri, Abdelaziz Sefiani
Format: Article
Language:English
Published: BMC 2019-08-01
Series:Journal of Medical Case Reports
Subjects:
Epilepsy
Clinical exome sequencing
SCN1A
SCN2A
Novel mutation
Moroccan
Online Access:http://link.springer.com/article/10.1186/s13256-019-2203-8

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http://link.springer.com/article/10.1186/s13256-019-2203-8

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