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Simon DB, Nelson-Williams C, Bia MJ, <i>et al<\/i>. Gitelman&apos;s variant of Bartter&apos;s syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet 1996; 12: 24-30.","DOI":"10.1038\/ng0196-24"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Cortesi C, Bettinelli A, Emma F, Fischbach M, Bertolani P, Bianchetti MG. Severe syncope and sudden death in children with inborn salt-losing hypokalaemic tubulopathies. Nephrol Dial Transplant 2005; 20: 1981-3.","DOI":"10.1093\/ndt\/gfh893"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Pachulski RT, Lopez F, Sharaf R. Gitelman&apos;s not-so-benign syndrome. N Engl J Med 2005; 353: 850-1.","DOI":"10.1056\/NEJMc051040"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Phan TT, Osman F, Jones A, El-Gaylani N. Ventricular tachycardia associated with hereditary magnesium-losing nephropathy. 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Heart Rhythm 2004; 1: 600-7.","DOI":"10.1016\/j.hrthm.2004.07.013"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Gouas L, Nicaud V, Berthet M, <i>et al<\/i>. Association of KCNQ1, KCNE1, KCNH2 and <i>SCN5A<\/i> polymorphisms with QTc interval length in a healthy population. Eur J Hum Genet 2005; 13: 1213-22.","DOI":"10.1038\/sj.ejhg.5201489"},{"key":"13","doi-asserted-by":"crossref","first-page":"912","DOI":"10.1016\/j.hrthm.2010.04.014","volume":"7","year":"2010","unstructured":"13. Tester DJ, Valdivia C, Harris-Kerr C, <i>et al<\/i>. Epidemiologic, molecular, and functional evidence suggest A572D-<i>SCN5A<\/i> should not be considered an independent LQT3-susceptibility mutation. Heart Rhythm 2010; 7: 912-9.","journal-title":"Heart Rhythm","ISSN":"http:\/\/id.crossref.org\/issn\/1547-5271","issn-type":"print"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Veltmann C, Barajas-Martinez H, Wolpert C, <i>et al<\/i>. Further insights in the most common <i>SCN5A<\/i> mutation causing overlapping phenotype of long QT syndrome, Brugada syndrome, and conduction defect. J Am Heart Assoc 2016; 5: e003379.","DOI":"10.1161\/JAHA.116.003379"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Matsumura H, Nakano Y, Ochi H, <i>et al<\/i>. H558R, a common <i>SCN5A<\/i> polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of <i>SCN5A<\/i> promoters. 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