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Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations
The Brugada syndrome is characterized by ST segment elevation in the right precodial leads V1-V3 on surface ECG accompanied by episodes of ventricular fibrillation causing syncope or even sudden death. The molecular and cellular mechanisms that lead to Brugada syndrome are not yet completely underst...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2653527/ https://ncbi.nlm.nih.gov/pubmed/19272188 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1423-0127-16-23 |
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