Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+)
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology,General Medicine
Reference41 articles.
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1. Genotypic and phenotypic characteristics of sodium channel—associated epilepsy in Chinese population;Journal of Human Genetics;2024-06-17
2. Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights;Journal of Neurology;2024-04-12
3. The Genetic Facets of Dravet Syndrome: Recent Insights;Annals of Child Neurology;2024-04-01
4. Clinical heterogeneity of epilepsy and mutation spectrum of voltage-gated sodium channel genes;2024-01-02
5. Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients;Frontiers in Neurology;2023-12-18
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