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Brugada syndrome genetics is associated with phenotype severity
AIMS : Brugada syndrome (BrS) is associated with an increased risk of sudden cardiac death due to ventricular tachycardia/fibrillation (VT/VF) in young, otherwise healthy individuals. Despite SCN5A being the most commonly known mutated gene to date, the genotype–phenotype relationship is poorly unde...
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| Publicado no: | Eur Heart J |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7955973/ https://ncbi.nlm.nih.gov/pubmed/33221895 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehaa942 |
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