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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...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2945207/ https://ncbi.nlm.nih.gov/pubmed/20877689 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0975-3583.64437 |
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