APA

Burgess D. E., Bartos D. C., Reloj A. R., Campbell K. S., Johnson J. N., Tester D. J., Ackerman M. J., Fressart V., Denjoy I., Guicheney P., Moss A. J., Ohno S., Horie M. & Delisle B. P. (20130221). High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. : Biochemistry.

Chicago

Burgess Don E, Bartos Daniel C, Reloj Allison R, Campbell Kenneth S, Johnson Jonathan N, Tester David J, Ackerman Michael J, Fressart Véronique, Denjoy Isabelle, Guicheney Pascale, Moss Arthur J, Ohno Seiko, Horie Minoru and Delisle Brian P. 20130221. High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. : Biochemistry.

Harvard

Burgess D. E., Bartos D. C., Reloj A. R., Campbell K. S., Johnson J. N., Tester D. J., Ackerman M. J., Fressart V., Denjoy I., Guicheney P., Moss A. J., Ohno S., Horie M. and Delisle B. P. (20130221). High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. : Biochemistry.

MLA

Burgess Don E, Bartos Daniel C, Reloj Allison R, Campbell Kenneth S, Johnson Jonathan N, Tester David J, Ackerman Michael J, Fressart Véronique, Denjoy Isabelle, Guicheney Pascale, Moss Arthur J, Ohno Seiko, Horie Minoru and Delisle Brian P. High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. : Biochemistry. 20130221.