Publications
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Filters: Author is Priori, Silvia G [Clear All Filters]
, “Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels.”, Am J Physiol Heart Circ Physiol, vol. 300, no. 1, pp. H288-99, 2011.
, “Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.”, Can J Cardiol, vol. 20, no. 4, pp. 425-30, 2004.
, “A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia.”, J Cardiovasc Electrophysiol, vol. 14, no. 4, pp. 407-11, 2003.
