Updates on the Inherited Cardiac Ion Channelopathies: From Cell to Clinical
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11936-012-0198-1.pdf
Reference57 articles.
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2. Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G, et al. Prevalence of the congenital long-QT syndrome. Circulation. 2009;120(18):1761–7. This is the first population-based study investigating the prevalence of congenital long QT syndrome in Caucasian infants.
3. Itoh H, Shimizu W, Hayashi K, Yamagata K, Sakaguchi T, Ohno S, et al. Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study. Hear Rhythm. 2010;7(10):1411–8. This multicenter study out of Japan compared genotyped patients with single versus compound mutations and found that those patients with compound mutations were more likely to have severe phenotypes.
4. Kanters JK, Fanoe S, Larsen LA, Bloch Thomsen PE, Toft E, Christiansen M. T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome. Hear Rhythm. 2004;1(3):285–92.
5. Jonathan NJ, Michael JA. The prevalence and diagnostic/prognostic utility of sinus arrhythmia in the evaluation of congenital long QT syndrome. Hear Rhythm. 2010;7(12):1785–9.
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2. Direct Measurement of Cardiac Na + Channel Conformations Reveals Molecular Pathologies of Inherited Mutations;Circulation: Arrhythmia and Electrophysiology;2015-10
3. Ion Channel Associated Diseases: Overview of Molecular Mechanisms;Chemical Reviews;2012-11-14
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