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
Cardiac ion channel gene mutations in Greek long QT syndrome patients
β Scribed by C -M. Kotta; A. Anastasakis; K. Gatzoulis; J. Papagiannis; P. Geleris; C. Stefanadis
- Publisher
- Springer-Verlag
- Year
- 2010
- Tongue
- English
- Weight
- 98 KB
- Volume
- 51
- Category
- Article
- ISSN
- 1234-1983
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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
Long QT syndrome (LQTS) is a heterogeneous disorder caused by mutations of at least five different loci. Three of these, LQT1, LQT2, and LQT5, encode potassium channel subunits. LQT3 encodes the cardiac-specific sodium channel, SCN5A. Previously reported LQTS-associated mutations of SCN5A include a