REFERENCES
1. Chen J, Makiyama T, Wuriyanghai Y, Ohno S, Sasaki K, Hayano M, et al. Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction. Heart Rhythm. 2016;13(1):289-98.
2. Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, et al. Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome. Hum Genet. 1998;102(4):435-9.
3. Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet. 1996;12(1):17-23.
4. Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace. 2013 Oct;15(10):1389-406.
5. Refaat MM, Hotait M, Tseng ZH: Utility of the Exercise Electrocardiogram Testing in Sudden Cardiac Death Risk Stratification. Ann Noninvasive Electrocardiol 2014; 19(4): 311-318.
6. Refaat MM, Hotait M, London B: Genetics of Sudden Cardiac Death. Curr Cardiol Rep Jul 2015; 17(7): 606.
7. Steffensen AB, Refaat MM, David JP, Mujezinovic A, Calloe K, Wojciak J, et al. High Incidence of Functional Ion Channel Abnormalities in a Consecutive Long QT Syndrome Cohort with Genetic Variants of Unknown Significance. Sci Rep Jun 2015; 5: 10009.
8. Hammami Bomholtz S, Refaat M, Buur Steffensen A, David J, Espinosa K, Nussbaum R, et al. Functional phenotype variations of two novel KV7.1 mutations identified in patients with Long QT syndrome. Pacing Clin Electrophysiol Feb 2020; 43 (2): 210-216.
9. Refaat MM, El Hage L, Buur Steffensen A, Hotait M, Schmitt N, Scheinman MM, et al. Iron Overload Leading to Torsades de Pointes in β-Thalassemia and Long QT syndrome. Card Electrophysiol Clin Mar 2016; 8(1): 247-56.
10. Poulsen KL, Hotait M, Calloe K, Klaerke DA, Rebeiz A, Nemer G, et al. The mutation p.T613A in the pore helix of the KV11.1 potassium channel is associated with long QT syndrome. Pacing Clin Electrophysiol Nov 2015; 38(11):1304-9.
11. Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, et al. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. Circulation. 2001;103(1):89-95.
12. Kurokawa J, Chen L, Kass RS. Requirement of subunit expression for cAMP-mediated regulation of a heart potassium channel. Proceedings of the National Academy of Sciences. 2003;100(4):2122-7.
13. Priori SG, Napolitano C, Schwartz PJ, Grillo M, Bloise R, Ronchetti E, et al. Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers. Jama. 2004;292(11):1341-4.
14. Shimizu W, Moss AJ, Wilde AA, Towbin JA, Ackerman MJ, January CT, et al. Genotype-phenotype aspects of type 2 long QT syndrome. J Am Coll Cardiol. 2009;54(22):2052-62.