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The diagnosis and treatment of cardiac ion channelopathies: Congenital long QT syndrome and Brugada syndrome

✍ Scribed by Ryan G. Aleong; David J. Milan; Patrick T. Ellinor

Book ID
107555833
Publisher
Springer
Year
2007
Tongue
English
Weight
129 KB
Volume
9
Category
Article
ISSN
1092-8464

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The original article to which this Erratum refers was published in Human Mutation 20:382-391 (2003) The following errors were noticed in the original version of this article in Tables 4 and5 and in the section Results, subsections '' Analysis of KCNQ1'' and '' Analysis of KCNH2''. Within the manuscr

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Congenital long QT syndrome (LQTS) is electrocardiographically characterized by a prolonged QT interval and polymorphic ventricular arrhythmias (torsade de pointes). As a result of these arrhythmias, patients suffer from recurrent syncopes, seizures, or sudden death as the most dramatic event. Mutat