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Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: From the cradle to the bench. <i>J Cardiovasc Electrophysiol<\/i> 2014; 25: 66\u201373.","DOI":"10.1111\/jce.12270"},{"key":"28","doi-asserted-by":"crossref","unstructured":"28. Wei J, Wang DW, Alings M, Fish F, Wathen M, Roden DM, et al. Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na<sup>+<\/sup> channel. <i>Circulation<\/i> 1999; 99: 3165\u20133171.","DOI":"10.1161\/01.CIR.99.24.3165"},{"key":"29","doi-asserted-by":"crossref","unstructured":"29. Desch\u00eanes I, Baroudi G, Berthet M, Barde I, Chalvidan T, Denjoy I, et al. Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512 W and R1432G) syndromes. <i>Cardiovasc Res<\/i> 2000; 46: 55\u201365.","DOI":"10.1016\/S0008-6363(00)00006-7"},{"key":"30","doi-asserted-by":"crossref","unstructured":"30. 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