Clinical and functional reappraisal of alleged type 5 long QT syndrome: Causative genetic variants in the KCNE1-encoded minK β-subunit
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Reference21 articles.
1. Precision cardiovascular medicine: state of genetic testing;Giudicessi;Mayo Clin Proc,2017
2. Genotype- and phenotype-guided management of congenital long QT syndrome;Giudicessi;Curr Probl Cardiol,2013
3. Long QT syndrome type 5-Lite: defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant;Lane;Heart Rhythm,2018
4. The genetic architecture of long QT syndrome: a critical reappraisal;Giudicessi;Trends Cardiovasc Med,2018
5. Reappraisal of reported genes for sudden arrhythmic death;Hosseini;Circulation,2018
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