Sudden cardiac death without structural heart disease: Update on the long QT and brugada syndromes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11886-005-0088-1.pdf
Reference54 articles.
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2. Wang Q, Shen J, Splawski I, et al.: SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995, 80:805–811.
3. Sanguinetti MC, Jiang C, Curran ME, et al.: 1995. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. Cell 1995, 81:299–307.
4. Wang Q, Curran ME, Splawski I, et al.: Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 1996, 12:17–23.
5. Westenskow P, Splawski I, Timothy KW, et al.: Compound mutations: a common cause of severe long-QT syndrome. Circulation 2004, 109:1834–1841. The paper shows that LQTS-associated compound mutations cause a severe phenotype and are more common than expected.
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