Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes-Reference-Cited by-同舟云学术

Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes

Published:2014-04-12 Issue:12 Volume:16 Page:1828-1837
ISSN:1532-2092
Container-title:EP Europace
language:en
Short-container-title:

Author:

Fukuyama Megumi,Wang Qi,Kato Koichi,Ohno Seiko,Ding Wei-Guang,Toyoda Futoshi,Itoh Hideki,Kimura Hiromi,Makiyama Takeru,Ito Makoto,Matsuura Hiroshi,Horie Minoru

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/europace/article-pdf/16/12/1828/17428111/euu063.pdf

Reference19 articles.

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2. Prevalence of the congenital long-QT syndrome;Schwartz;Circulation,2009

3. Impact of genetics on the clinical management of channelopathies;Schwartz;J Am Coll Cardiol,2013

4. Structure and function of voltage-gated sodium and calcium channels;Catterall;Curr Opin Neurobiol,1991

5. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism;Splawski;Cell,2004

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