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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...
שמור ב:
| הוצא לאור ב: | Int J Cardiol Heart Vasc |
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| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Elsevier
2020
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| נושאים: | |
| גישה מקוונת: | 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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