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High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K+ permeation
Don E. Burgess, Daniel C. Bartos, Allison R. Reloj, Kenneth S. Campbell, Jonathan N. Johnson, David J. Tester, Michael J. Ackerman, Véronique Fressart, Isabelle Denjoy, Pascale Guicheney, Arthur J. Moss, Seiko Ohno, Minoru Horie, Brian P. Delisle
Research output: Contribution to journal › Article › peer-review
14
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