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.

@article{Lehnart2007InheritedAA,
  title={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.},
  author={Stephan E. Lehnart and Michael J. Ackerman and D Woodrow Benson and Ramon Brugada and Colleen E. Clancy and J Kevin Donahue and Alfred L George and Augustus O. Grant and Stephen C. Groft and Craig T. January and David A. Lathrop and W Jonathan Lederer and Jonathan C. Makielski and Peter J. Mohler and Arthur J. Moss and Jeanne M Nerbonne and Timothy Olson and Dennis A. Przywara and Jeffrey Allen Towbin and Lan-Hsiang Wang and Andrew Robert Marks},
  journal={Circulation},
  year={2007},
  volume={116 20},
  pages={2325-45}
}
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 to other inherited arrhythmogenic mechanisms. Another major goal was to provide… CONTINUE READING
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