Publications
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Filtres: Author is Deschênes, Isabelle [Enlever les filtres]
« A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope. », Heart Rhythm, vol. 5, nᵒ 11, p. 1577-86, 2008.
, « SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene. », Circulation, vol. 114, nᵒ 5, p. 368-76, 2006.
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