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Cellular Basis for Arrhythmogenesis in an Experimental Model of the SQT1 Form of the Short QT Syndrome
BACKGROUND: Short QT syndrome (SQT) is a primary electrical disease associated with a high risk of sudden cardiac death. A gain-of-function in I(Kr), due to a mutation in KCNH2, underlies SQT1. OBJECTIVE: To examine the cellular basis for arrhythmogenesis in an experimental model of SQT1 created usi...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2008
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2361425/ https://ncbi.nlm.nih.gov/pubmed/18362027 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2008.01.022 |
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