⌘+K

Pulse Explore Communities Researchers Journals

Home Communities Explore

February 10, 2024

[Clinical features and genetic analysis of five children with epilepsies due to variants of SCN8A gene].

Xin Zhang Shiyan Qiu Yang Li Yufen Li Na Xu Xixi Yu

View at Publisher

Ask AI

Bookmark

Share

Abstract

To explore the clinical and genetic characteristics of five children with epilepsies due to variants of SCN8A gene.

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Zhang et al. (2024) studied this question.

synapsesocial.com/papers/68e79c4cb6db64358770b681 https://doi.org/10.3760/cma.j.cn511374-20221020-00702

View at Publisher

Ask AI

Bookmark

Share

Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Clinical characteristics and genetic analysis of patients with SCN1A gene pathological variant-related disorders: a single-center retrospective studyCohort Study · 2026
2SCN1A-Related Epilepsy: Novel Mutations and Rare Phenotypescase_series · 2022 · 8 citations
3Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies2024 · 11 citations
4Novel SCN8A mutation in a girl with refractory seizures and autistic featurescase_report · 2017 · 2 citations
5[Correlation between clinical phenotypes and genotypes among 46 children with SCN1A-related developmental epileptic encephalopathy].2024

More related papers

SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations2024
Case Report: Novel Homozygous Likely Pathogenic SCN1A Variant With Autosomal Recessive Inheritance and Review of the Literature2021
Unusual Voltage-Gated Sodium and Potassium Channelopathies Related to Epilepsy2024