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Wilde, A.A.* et al.: Clinical aspects of type 3 long QT syndrome: An international multicenter study. Circulation 134, 872-882 (2016)
Behr, E.R.* et al.: Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovasc. Res. 106, 520-529 (2015)
de Ferrari, G.M.* et al.: Clinical management of catecholaminergic polymorphic ventricular tachycardia: The role of left cardiac sympathetic denervation. Circulation 131, 2185-2193 (2015)
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
Boczek, N.J.* et al.: Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome. Circ. Res. 115, 460-469 (2014)
Crotti, L. et al.: Long QT syndrome-associated mutations in intrauterine fetal death. JAMA 309, 1473-1482 (2013)
Hennessey, J.A.* et al.: FGF12 is a candidate Brugada syndrome locus. Heart Rhythm 10, 1886-1894 (2013)
Amin, A.S.* et al.: Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner. Eur. Heart J. 33, 714-723 (2012)
Chockalingam, P.* et al.: Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: Higher recurrence of events under metoprolol. J. Am. Coll. Cardiol. 60, 2092-2099 (2012)
Crotti, L. et al.: Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada Syndrome genetic testing: Implications for genetic testing. J. Am. Coll. Cardiol. 60, 1410-1418 (2012)
Hu, D.* et al.: A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents. Heart Rhythm 9, 760-769 (2012)
Ishikawa, T.* et al.: A novel disease gene for Brugada syndrome: Sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5. Circ.-Arrhythmia Electrophysiol. 5, 1098-1107 (2012)