Associated Papers
Clinical and Genetic Spectrum of Patients with Pediatric-Onset Epilepsy: Insights from a Single-Center Study.
Tozkir H et al.
Genes, 2025
Biallelic SCN1A variants with divergent epilepsy phenotypes.
Pentz R et al.
Seizure, 2025
Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome.
Teralı K et al.
Clinical and Translational Science, 2024
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