Novel<i>SCN5A</i>Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French FamilyFlorence Kyndt, Hervé Le Marec, Vincent Probst et al.|Circulation|2001Cited by 368
Conditional Mineralocorticoid Receptor Expression in the Heart Leads to Life-Threatening ArrhythmiasAntoine Ouvrard‐Pascaud, Frédéric Jaisser, Pierre Maison‐Blanche et al.|Circulation|2005Cited by 264
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node diseaseSolena Le Scouarnec, Peter J. Mohler, Naina Bhasin et al.|Proceedings of the National Academy of Sciences|2008Cited by 174
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre diseaseVincent Probst, Hervé Le Marec, Florence Kyndt et al.|Journal of the American College of Cardiology|2003Cited by 173
Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse ModelAnne‐Laure Léoni, Flavien Charpentier, Bruno Gavillet et al.|PLoS ONE|2010Cited by 82