Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference24 articles.
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2. Natural history of Brugada syndrome: insights for risk stratification and management;Priori;Circulation,2002
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4. The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis;Medeiros-Domingo;J Am Coll Cardiol,2009
5. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing;Kapplinger;Heart Rhythm,2009
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