QuickView for SCN3B;jsessionid=67984B18A7CAB402C88C48147F7FB671 (gene)

1. Identification of a novel Scn3b mutation in a Chinese Brugada syndrome pedigree: implications for Na…
2. Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function…
3. miR-190a-5p Partially Represses the Abnormal Electrical Activity of SCN3B in Cardiac Arrhythmias by …
4. Mapping protein interactions of sodium channel NaV1.7 using epitope-tagged gene-targeted mice.
5. Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fi…

There were no clinical trials for SCN3B;jsessionid=67984B18A7CAB402C88C48147F7FB671