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Genetic analysis of Brugada syndrome and congenital long-QT syndrome type 3 in the Chinese
BACKGROUND: Brugada syndrome and congenital long-QT syndrome (LQTS) type 3 (LQT3) are 2 inherited conditions of abnormal cardiac excitability characterized clinically by an increased risk of ventricular tachyarrhythmias. SCN5A gene that encodes the cardiac sodium channel α subunit is responsible for...
| Autores principales: | , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2945207/ https://www.ncbi.nlm.nih.gov/pubmed/20877689 http://dx.doi.org/10.4103/0975-3583.64437 |