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History
- Received August 5, 2003
- Accepted September 2, 2003
- Published online November 26, 2003.
Article Versions
- Earlier version (October 15, 2003 - 13:05).
- You are viewing the most recent version of this article.
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The American Society for Pharmacology and Experimental Therapeutics
Author Information
- Arun Anantharam,
- Steven M. Markowitz and
- Geoffrey W. Abbott
- Division of Cardiology, Department of Medicine (A.A., S.M.M., G.W.A.); Graduate Program in Neuroscience (A.A.); Department of Pharmacology (G.W.A.); Weill Medical College of Cornell University, New York, New York
- Address correspondence to:
Dr. Geoffrey W. Abbott, Division of Cardiology, Dept. of Medicine, Weill Medical College of Cornell University, Starr 463, 520 East 70th Street, New York, NY 10021. E-mail: gwa2001{at}med.cornell.edu
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In this issue
Pharmacogenetic Considerations in Diseases of Cardiac Ion Channels
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- Article
- Abstract
- Cardiac Ion Currents and Arrhythmia
- KCNQ1 and MinK Mutations Cause Inherited Long QT Syndrome and Deafness
- HERG and MiRP1 Mutations Associate with Inherited Long QT Syndrome
- HERG and MiRP1 Are Key Molecular Determinants in Acquired Long QT Syndrome
- Lethal Mutations and Subtle SNPs in the SCN5A Gene
- Gene-Guided Therapies
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