Title: Syncope in Hereditary Arrhythmogenic Syndromes
Abstract: Since the discovery of the first mutation causing long QT syndrome (LQTS) in 1995, the field of hereditary arrhythmogenic syndromes has expanded greatly. Today, these syndromes include LQTS, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. There is also evidence suggesting that the newly described malignant early repolarization syndrome also has a genetic cause.
Publication Year: 2013
Publication Date: 2013-11-12
Language: en
Type: article
Indexed In: ['crossref']
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Cited By Count: 1
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