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 Hospit...

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Autors principals:	Tong Zhao, Fang Chen, Le Wang, Yun Xie, Minglei Yang, Fan Feng
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2025-06-01
Col·lecció:	Italian Journal of Pediatrics
Matèries:	Children Epilepsy SCN2A Clinical features Gene mutation Inheritance
Accés en línia:	https://doi.org/10.1186/s13052-025-02009-4
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