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HERG1 Channel Agonists and Cardiac Arrhythmia
Type 1 human ether-a-go-go-related gene (hERG1) potassium channels are a key determinant of normal repolarization of cardiac action potentials. Loss of function mutations in hERG1 channels cause inherited long QT syndrome and increased risk of cardiac arrhythmia and sudden death. Many common medicat...
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| Formato: | Artigo |
| Idioma: | Inglês |
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2013
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3984452/ https://ncbi.nlm.nih.gov/pubmed/24721650 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.coph.2013.11.006 |
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