QuickView for SCN3B;jsessionid=9D73E4CDFD80E291BA55482A26A1374F;jsessionid=C7331604F466D0FA74897768FF39D659;jsessionid=576685C62FD97B263A1D9DB240F13609;jsessionid=690C7DBECF1645FBEC7F6A4F8489657C (gene)

1. Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function…
2. miR-190a-5p Partially Represses the Abnormal Electrical Activity of SCN3B in Cardiac Arrhythmias by …
3. Mapping protein interactions of sodium channel NaV1.7 using epitope-tagged gene-targeted mice.
4. Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fi…
5. Effects of GRM4, SCN2A and SCN3B polymorphisms on antiepileptic drugs responsiveness and epilepsy su…

There were no clinical trials for SCN3B;jsessionid=9D73E4CDFD80E291BA55482A26A1374F;jsessionid=C7331604F466D0FA74897768FF39D659;jsessionid=576685C62FD97B263A1D9DB240F13609;jsessionid=690C7DBECF1645FBEC7F6A4F8489657C