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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
- Footnotes
- References
- Figures & Data
- Info & Metrics
- eLetters
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