Studies of Magnesium in Congenital Long QT Syndrome
β Scribed by K. Hoshino; K. Ogawa; T. Hishitani; R. Kitazawa
- Publisher
- Springer
- Year
- 2002
- Tongue
- English
- Weight
- 165 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0172-0643
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π SIMILAR VOLUMES
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
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