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QuickView for Nav1.4 (gene)
Most Relevant Literature
- A Sodium Channel Myotonia Presenting with Intermittent Dysphagia as a Manifestation of a Rare SCN4A …
- A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.
- Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene.
- Paramyotonia congenita caused by a novel mutation of SCN4A gene in a Chinese family].
- Mefloquine inhibits voltage dependent Nav1.4 channel by overlapping the local anaesthetic binding si…
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…
- Effects of Mexiletine on Colonic Transit in a Patient With Irritable Bowel Syndrome - Constipation (…
- Use of Topical Lidocaine to Reduce Pain in Patients With Diabetic Neuropathy
- Depolarising Electrical Skin Stimulation in Neuropathic and Postoperative Pain
