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- W2043133750 startingPage "S49" @default.
- W2043133750 abstract "Inherited primary arrhythmias, namely congenital long QT syndrome, Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia, account for a significant proportion of sudden cardiac deaths in young and apparently healthy individuals. Genetic testing plays an integral role in the diagnosis, risk-stratification and treatment of probands and family members. It is increasingly obvious that collaborative efforts are required to understand and manage these relatively rare but potentially lethal diseases. This article aims to update readers on the recent developments in our knowledge of inherited arrhythmias and to lay the foundation for a national synergistic effort to characterize them in the Indian population." @default.
- W2043133750 created "2016-06-24" @default.
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- W2043133750 date "2014-01-01" @default.
- W2043133750 modified "2023-10-18" @default.
- W2043133750 title "Inherited arrhythmia syndromes leading to sudden cardiac death in the young: A global update and an Indian perspective" @default.
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- W2043133750 doi "https://doi.org/10.1016/j.ihj.2013.11.008" @default.
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