Unraveling the influence of genomic context on pleiotropy in SCN5A-mediated cardiac channelopathies: Insights from the Worm Study
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Reference14 articles.
1. Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes;Giudicessi;Transl Res,2013
2. Clinical spectrum of SCN5A mutations: long QT syndrome, Brugada syndrome, and cardiomyopathy;Wilde;JACC Clin Electrophysiol,2018
3. The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome;Makita;J Clin Invest,2008
4. Purkinje system hyperexcitability and ventricular arrhythmia risk in type 3 long QT syndrome;Barake;Heart Rhythm,2020
5. Further insights in the most common SCN5A mutation causing overlapping phenotype of long QT syndrome, Brugada syndrome, and conduction defect;Veltmann;J Am Heart Assoc,2016
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