Genotype-Phenotype Aspects of Type 2 Long QT Syndrome-Reference-Cited by-同舟云学术

Genotype-Phenotype Aspects of Type 2 Long QT Syndrome

Published:2009-11 Issue:22 Volume:54 Page:2052-2062
ISSN:0735-1097
Container-title:Journal of the American College of Cardiology
language:en
Short-container-title:Journal of the American College of Cardiology

Author:

Shimizu Wataru,Moss Arthur J.,Wilde Arthur A.M.,Towbin Jeffrey A.,Ackerman Michael J.,January Craig T.,Tester David J.,Zareba Wojciech,Robinson Jennifer L.,Qi Ming,Vincent G. Michael,Kaufman Elizabeth S.,Hofman Nynke,Noda Takashi,Kamakura Shiro,Miyamoto Yoshihiro,Shah Samit,Amin Vinit,Goldenberg Ilan,Andrews Mark L.,McNitt Scott

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference30 articles.

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3. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome;Curran;Cell,1995

4. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel;Sanguinetti;Cell,1995

5. Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2;January;J Cardiovasc Electrophysiol,2000

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