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Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias

The congenital long QT syndrome is a rare disorder in which mutation carriers are at risk for polymorphic ventricular tachycardia and/or sudden cardiac death. Discovery and analysis of gene mutations associated with variants of this disorder have provided novel insight into mechanisms of cardiac arr...

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Detalhes bibliográficos
Main Authors: Kass, Robert S., Moss, Arthur J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2003
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC193679/
https://ncbi.nlm.nih.gov/pubmed/12975462
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200319844
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