A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation-Reference-Cited by-同舟云学术

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A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation

Published:2013-08-30 Issue:3 Volume:466 Page:529-540
ISSN:0031-6768
Container-title:Pflügers Archiv - European Journal of Physiology
language:en
Short-container-title:Pflugers Arch - Eur J Physiol

Author:

Ki Chang-Seok,Jung Chae Lim,Kim Hyun-ji,Baek Kwan-Hyuck,Park Seung Jung,On Young Keun,Kim Ki-Suk,Noh Su Jin,Youm Jae Boum,Kim June Soo,Cho Hana

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Clinical Biochemistry,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s00424-013-1337-6.pdf

Reference31 articles.

1. Andalib A, Brugada R, Nattel S (2008) Atrial fibrillation: evidence for genetically determined disease. Curr Opin Cardiol 23(3):176–183. doi: 10.1097/HCO.0b013e3282fa7142

2. Barhanin J, Lesage F, Guillemare E, Fink M, Lazdunski M, Romey G (1996) K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current. Nature 384(6604):78–80. doi: 10.1038/384078a0

3. Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP (2013) A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation. J Cardiovasc Electrophysiol 24 (5):562–569. doi:10.1111/jce.12068 [doi]

4. Bartos DC, Duchatelet S, Burgess DE, Klug D, Denjoy I, Peat R, Lupoglazoff JM, Fressart V, Berthet M, Ackerman MJ, January CT, Guicheney P, Delisle BP (2011) R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. Heart Rhythm 8(1):48–55. doi: 10.1016/j.hrthm.2010.09.010

5. Chan PJ, Osteen JD, Xiong D, Bohnen MS, Doshi D, Sampson KJ, Marx SO, Karlin A, Kass RS (2012) Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1. J Gen Physiol 139 (2):135–144. doi:jgp.201110672 [pii] 10.1085/jgp.201110672 [doi]

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