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LQTS Mutation N1325S in Cardiac Sodium Channel Gene SCN5A Causes Cardiomyocyte Apoptosis, Cardiac Fibrosis and Contractile Dysfunction in Mice

OBJECTIVE: Mutations in the cardiac sodium channel gene SCN5A cause long QT syndrome (LQTS). We previously generated a LQTS mouse model (TG-NS) that overexpresses LQTS mutation N1325S in SCN5A. The TG-NS mice manifested the clinical features of LQTS including spontaneous VT, syncope and sudden death...

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Dettagli Bibliografici
Autori principali: Zhang, Teng, Yong, Sandro L., Drinko, Jeanne K., Popović, Zoran B., Shryock, John C., Belardinelli, Luiz, Wang, Qing Kenneth
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2009
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2891203/
https://ncbi.nlm.nih.gov/pubmed/19762097
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2009.08.047
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