Clinical and molecular genetics of the short QT syndrome
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Reference45 articles.
1. Sudden death in patients without structural heart disease;Wever;J Am Coll Cardiol,2004
2. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation;Chen;Nature,1998
3. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene;Keating;Science,1991
4. Molecular genetics of arrhythmias and cardiovascular conditions associated with arrhythmias;Antzelevitch;J Cardiovasc Electrophysiol,2003
5. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia;Priori;Circulation,2002
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