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pubmed-article:17984373pubmed:abstractTextThe impressive clinical heterogeneity of the long-QT syndrome (LQTS) remains partially unexplained. In a South African (SA) founder population, we identified a common LQTS type 1 (LQT1)-causing mutation (KCNQ1-A341V) associated with high clinical severity. We tested whether the arrhythmic risk was caused directly by A341V or by its presence in the specific ethnic setting of the SA families.lld:pubmed
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pubmed-article:17984373pubmed:articleTitleThe common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.lld:pubmed
pubmed-article:17984373pubmed:affiliationSection of Cardiology, Department of Lung, Blood and Heart, University of Pavia, Pavia, Italy.lld:pubmed
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