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- W2086839800 endingPage "186" @default.
- W2086839800 startingPage "173" @default.
- W2086839800 abstract "Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disease caused by mutations in genes coding for cardiac sarcomeres. HCM is the most common inherited heart disease, with a prevalence of 0.2%. There are multiple genetic variants that cause pleomorphic clinical attributes and disease characterized by myocardial disarray and myocardial hypertrophy. Patients are at an increased risk of atrial and ventricular arrhythmias. Management of these arrhythmias is complex. Atrial fibrillation is associated with increased mortality and thromboembolism. Ventricular arrhythmias are life threatening and best treated with an implantable defibrillator." @default.
- W2086839800 created "2016-06-24" @default.
- W2086839800 creator A5024827353 @default.
- W2086839800 creator A5061856321 @default.
- W2086839800 creator A5077914816 @default.
- W2086839800 date "2015-06-01" @default.
- W2086839800 modified "2023-10-18" @default.
- W2086839800 title "Atrial and Ventricular Arrhythmias in Hypertrophic Cardiomyopathy" @default.
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- W2086839800 doi "https://doi.org/10.1016/j.ccep.2015.03.002" @default.
- W2086839800 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26002384" @default.