Associated Papers
SCN1Bβ mutations that affect their association with Kv4.3 underlie early repolarization syndrome.
Yao H et al.
Journal of Cellular and Molecular Medicine, 2018
Multiple genetic variations in sodium channel subunits in a case of sudden infant death syndrome.
Denti F et al.
Pacing and Clinical Electrophysiology : Pace, 2018
Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.
Yuan L et al.
American Journal of Physiology. Heart and Circulatory Physiology, 2014
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