Flecainide Provocation Reveals Concealed Brugada Syndrome in a Long QT Syndrome Family With a Novel L1786Q Mutation in SCN5A-Reference-Cited by-同舟云学术

Flecainide Provocation Reveals Concealed Brugada Syndrome in a Long QT Syndrome Family With a Novel L1786Q Mutation in SCN5A

Published:2014 Issue:5 Volume:78 Page:1136-1143
ISSN:1346-9843
Container-title:Circulation Journal
language:en
Short-container-title:Circ J

Author:

Kanters Jørgen K.¹²,Yuan Lei¹,Hedley Paula L.³⁴,Stoevring Birgitte³,Jons Christian²,Bloch Thomsen Poul Erik²,Grunnet Morten¹⁵,Christiansen Michael³,Jespersen Thomas¹

Affiliation:

1. Danish National Foundation Research Centre in Arrhythmias (DARC), Laboratory of Experimental Cardiology, Department of Biomedical Sciences

2. Department of Cardiology P, Gentofte University Hospital

3. Statens Serum Institut

4. Department of Biomedical Sciences, University of Stellenbosch

5. NeuroSearch

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/circj/78/5/78_CJ-13-1167/_pdf

Reference35 articles.

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2. 2. Tfelt-Hansen J, Winkel BG, Grunnet M, Jespersen T. Inherited cardiac diseases caused by mutations in the Nav1.5 sodium channel. J Cardiovasc Electrophysiol 2009; 21: 107–115.

3. 3. Hedley PL, Jorgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, et al. The genetic basis of Brugada syndrome: A mutation update. Hum Mutat 2009; 30: 1256–1266.

4. 4. Berne P, Brugada J. Brugada syndrome 2012. Circ J 2012; 76: 1563–1571.

5. 5. Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baro I, et al. Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family. Circulation 2001; 104: 3081–3086.

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