Associated Papers
SCN5A Cardiomyopathy: from Ion Channel Dysfunction To Clinical Disease.
Heymans ABM et al.
Current Cardiology Reports, 2025
Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated SCN5A Variants: A Systematic Review.
Peters S et al.
Circulation. Genomic and Precision Medicine, 2022
Targeted deep sequencing analyses of long QT syndrome in a Japanese population.
Nagata Y et al.
Plos One, 2022
A Novel SCN5A Mutation Found in a Familial Case of Long QT Syndrome Complicated by Severe Left Ventricular Dysfunction.
Kimura M et al.
The Canadian Journal of Cardiology, 2017
The congenital long QT syndrome Type 3: An update.
Pérez-Riera AR et al.
Indian Pacing and Electrophysiology Journal, 0
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