The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: Toward a mutation-specific risk stratification

Lia Crotti, Carla Spazzolini, Peter J. Schwartz, Wataru Shimizu, Isabelle Denjoy, Eric Schulze-Bahr, Elena V. Zaklyazminskaya, Heikki Swan, Michael J. Ackerman, Arthur J. Moss, Arthur A.M. Wilde, Minoru Horie, Paul A. Brink, Roberto Insolia, Gaetano M. De Ferrari, Gabriele Crimi

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Medicine & Life Sciences