Associated Papers
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
Peeters U et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2015
SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients.
Ricci MT et al.
Scientific Reports, 2014
A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome.
Riuró H et al.
Heart Rhythm, 2014
Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy.
Refsgaard L et al.
Applied & Translational Genomics, 2012
Voltage-gated Na+ channel β1B: a secreted cell adhesion molecule involved in human epilepsy.
Patino GA et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2011
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