SCN5A Mutation associated with acute myocardial infarction

Ventricular tachycardia and fibrillation (VT/VF) complicating Brugada syndrome, a genetic disorder linked to SCN5A mutations, and VF complicating acute myocardial infarction (AMI) have both been linked to phase 2 reentry. Because of these mechanistic similarities in arrhythmogenesis, we examined the...

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Bibliografiset tiedot
Päätekijät: Oliva, Antonio, Hu, Dan, Viskin, Sami, Carrier, Tabitha, Cordeiro, Jonathan M., Barajas-Martinez, Hector, Wu, Yusheng, Burashnikov, Elena, Brugada, Ramon, Rosso, Rafael, Guerchicoff, Alexandra, Pollevick, Guido, Pascali, Vincenzo L., Antzelevitch, Charlie
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2813686/
https://ncbi.nlm.nih.gov/pubmed/19345130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.legalmed.2009.02.044
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