Inherited arrhythmias: A National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function

Stephan E. Lehnart, Michael J. Ackerman, D. Woodrow Benson, Ramon Brugada, Colleen E. Clancy, J. Kevin Donahue, Alfred L. George, Augustus O. Grant, Stephen C. Groft, Craig T. January, David A. Lathrop, W. Jonathan Lederer, Jonathan C. Makielski, Peter J. Mohler, Arthur Moss, Jeanne M. Nerbonne, Timothy M. Olson, Dennis A. Przywara, Jeffrey A. Towbin, Lan Hsiang WangAndrew R. Marks

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