Associated Papers
Toward precision medicine in SCN3A variants-associated encephalopathies and epilepsy: optimizing genetic diagnosis and molecular subregional effects.
Wang PY et al.
Frontiers in Neurology, 2026
Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).
Ma H et al.
Seizure, 2021
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