SCN2A gene mutations with epilepsy: single center experience

SCN2A gene mutations with epilepsy: single center experience

Abstract Background To explore the clinical phenotypic characteristics and genetic analysis of children with SCN2A gene mutation-related epilepsy. Methods A retrospective study of children with SCN2A gene mutation epilepsy admitted to the Department of Neurology of Hebei Provincial Children's H...

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Bibliographic Details
Main Authors: Tong Zhao, Fang Chen, Le Wang, Yun Xie, Minglei Yang, Fan Feng
Format: Article
Language:English
Published: BMC 2025-06-01
Series:Italian Journal of Pediatrics
Subjects:
Children
Epilepsy
SCN2A
Clinical features
Gene mutation
Inheritance
Online Access:https://doi.org/10.1186/s13052-025-02009-4
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