Publications
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Filters: Author is Delacrétaz, Etienne [Clear All Filters]
, “A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation.”, Cardiovasc Res, vol. 70, no. 3, pp. 521-9, 2006.
, “A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.”, J Mol Cell Cardiol, vol. 35, no. 12, pp. 1513-21, 2003.
