Publications
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Filtres: Author is Priori, Silvia G [Enlever les filtres]
, « 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, p. 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, p. 425-30, 2004.
, « A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia. », J Cardiovasc Electrophysiol, vol. 14, nᵒ 4, p. 407-11, 2003.
