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Brugada syndrome: A comprehensive review of pathophysiological mechanisms and risk stratification strategies
Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to ventricular arrhythmias and sudden cardiac death. Originally believed to be predominantly associated with mutations in SCN5A encoding for the cardiac sodium channel, mutations of 18 genes other than SCN5A have been impl...
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| Veröffentlicht in: | Int J Cardiol Heart Vasc |
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| Hauptverfasser: | , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6974766/ https://ncbi.nlm.nih.gov/pubmed/31993492 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcha.2020.100468 |
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