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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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Autors principals: Liang, Peng, Liu, Wenling, Li, Cuilan, Tao, Wuhua, Li, Lei, Hu, Dayi
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications 2010
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Accés en línia: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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