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Prevalence and clinical correlates of QT prolongation in patients with hypertrophic cardiomyopathy

AIMS: Congenital or acquired QT prolongation is a risk factor for life-threatening arrhythmias. In patients with hypertrophic cardiomyopathy (HCM), the QT interval may be intrinsically prolonged. However, the prevalence, cause, and significance of QT prolongation among patients with HCM are unknown....

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Main Authors: Johnson, Jonathan N., Grifoni, Camilla, Bos, J. Martijn, Saber-Ayad, Maha, Ommen, Steve R., Nistri, Stefano, Cecchi, Franco, Olivotto, Iacopo, Ackerman, Michael J.
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2011
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3086898/
https://ncbi.nlm.nih.gov/pubmed/21345853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehr021
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