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NOVEL MUTATION IN THE SCN5A GENE ASSOCIATED WITH ARRHYTHMIC STORM DEVELOPING DURING ACUTE MYOCARDIAL INFARCTION
BACKGROUND: Ventricular tachycardia and fibrillation (VT/VF) complicating Brugada syndrome, a genetic disorder linked to SCN5A mutations, and VF complicating acute myocardial infarction (AMI) have both been linked to phase 2 reentry. OBJECTIVE: Because of these mechanistic similarities in arrhythmog...
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| Hauptverfasser: | , , , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2007
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1978483/ https://ncbi.nlm.nih.gov/pubmed/17675083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2007.03.040 |
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