APA

Crotti L., Spazzolini C., Schwartz P. J., Shimizu W., Denjoy I., Schulze-Bahr E., Zaklyazminskaya E. V., Swan H., Ackerman M. J., Moss A. J., Wilde A. A. M., Horie M., Brink P. A., Insolia R., De Ferrari G. M. & Crimi G. (20071212). 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. : Circulation.

Chicago

Crotti Lia, Spazzolini Carla, Schwartz Peter J, Shimizu Wataru, Denjoy Isabelle, Schulze-Bahr Eric, Zaklyazminskaya Elena V, Swan Heikki, Ackerman Michael J, Moss Arthur J, Wilde Arthur A M, Horie Minoru, Brink Paul A, Insolia Roberto, De Ferrari Gaetano M and Crimi Gabriele. 20071212. 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. : Circulation.

Harvard

Crotti L., Spazzolini C., Schwartz P. J., Shimizu W., Denjoy I., Schulze-Bahr E., Zaklyazminskaya E. V., Swan H., Ackerman M. J., Moss A. J., Wilde A. A. M., Horie M., Brink P. A., Insolia R., De Ferrari G. M. and Crimi G. (20071212). 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. : Circulation.

MLA

Crotti Lia, Spazzolini Carla, Schwartz Peter J, Shimizu Wataru, Denjoy Isabelle, Schulze-Bahr Eric, Zaklyazminskaya Elena V, Swan Heikki, Ackerman Michael J, Moss Arthur J, Wilde Arthur A M, Horie Minoru, Brink Paul A, Insolia Roberto, De Ferrari Gaetano M and Crimi Gabriele. 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. : Circulation. 20071212.