Publications
Export 5 results:
Filters: Keyword is Death, Sudden, Cardiac and Author is Mohamed Chahine [Clear All Filters]
, “The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT.”, Gene, vol. 536, no. 2, pp. 348-56, 2014.
, “The Brugada syndrome in Canada: a unique French-Canadian experience.”, Can J Cardiol, vol. 23 Suppl B, p. 71B-75B, 2007.
, “Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).”, Circ Res, vol. 88, no. 12, pp. E78-83, 2001.
, “Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes.”, FEBS Lett, vol. 487, no. 2, pp. 224-8, 2000.
, “Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.”, Cardiovasc Res, vol. 46, no. 1, pp. 55-65, 2000.
