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.

doi:10.1161/CIRCULATIONAHA.107.711689

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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.

Circulation - 13 Nov 2007

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

Abstract excerpt

The National Heart, Lung, and Blood Institute and Office of Rare Diseases at the National Institutes of Health organized a workshop (September 14 to 15, 2006, in Bethesda, Md) to advise on new research directions needed for improved identification and treatment of rare inherited arrhythmias. These included the following: (1) Na+ channelopathies; (2) arrhythmias due to K+ channel mutations; and (3) arrhythmias due...

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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.

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