KCNH2 -K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome-Reference-Cited by-同舟云学术

KCNH2 -K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome

Published:2005-08-30 Issue:9 Volume:112 Page:1251-1258
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Crotti Lia¹,Lundquist Andrew L.¹,Insolia Roberto¹,Pedrazzini Matteo¹,Ferrandi Chiara¹,De Ferrari Gaetano M.¹,Vicentini Alessandro¹,Yang Ping¹,Roden Dan M.¹,George Alfred L.¹,Schwartz Peter J.¹

Affiliation:

1. From the Department of Cardiology (L.C., G.M.D.F., A.V., P.J.S.), University of Pavia, and IRCCS Policlinico S. Matteo, Pavia; Molecular Cardiology Laboratory (L.C., R.I., M.P., C.F., P.J.S.), IRCCS Policlinico S. Matteo, Pavia, Italy; and the Departments of Pharmacology (A.L.L., P.Y., D.M.R., A.L.G.) and Medicine (D.M.R., A.L.G.), Vanderbilt University, Nashville, Tennessee.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference39 articles.

1. The long Q-T syndrome

2. Schwartz PJ Priori SG Napolitano C. The long QT syndrome. In: Zipes DP Jalife J eds. Cardiac Electrophysiology: From Cell to Bedside. 3rd ed. Philadelphia Pa: WB Saunders Co; 2000: 597–615.

3. CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism

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