QuickView for SCN2B;jsessionid=2B91FF81A8B8E71375BF56E50AFC7BDD (gene)

1. SCN1B and SCN2B gene variants analysis in dravet syndrome patients: Analysis of 22 cases.
2. Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
3. The voltage-gated sodium channel β2 subunit associates with lipid rafts by S-palmitoylation.
4. A novel gain-of-function sodium channel β2 subunit mutation in idiopathic small fiber neuropathy.
5. SCN2B in the Rat Trigeminal Ganglion and Trigeminal Sensory Nuclei.

There were no clinical trials for SCN2B;jsessionid=2B91FF81A8B8E71375BF56E50AFC7BDD