Associated Papers
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
El-Battrawy I et al.
Frontiers in Cell and Developmental Biology, 2019
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
Select a paper to view details