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