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QuickView for NaV1.2 (gene)
Most Relevant Literature
- Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties.
- Inhibitory effect of atomoxetine on Nav1.2 voltage-gated sodium channel currents.
- Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons.
- A mutation in the neonatal isoform of SCN2A causes neonatal-onset epilepsy.
- Functional correlates of clinical phenotype and severity in recurrent SCN2A variants.
Most Relevant Clinical Trials
- Carbamazapine for Inherited Erythromelalgia Patients With NaV1.7 Mutations
- Safety and Tolerability of Lacosamide in Patients With Gain-of-function Nav1.7 Mutations Related Sma…
- Probing the Role of Sodium Channels in Painful Neuropathies
- Depolarising Electrical Skin Stimulation in Neuropathic and Postoperative Pain
- Use of Topical Lidocaine to Reduce Pain in Patients With Diabetic Neuropathy
