Impact of Genetics on the Clinical Management of Channelopathies-Reference-Cited by-同舟云学术

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Impact of Genetics on the Clinical Management of Channelopathies

Published:2013-07 Issue:3 Volume:62 Page:169-180
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:

Schwartz Peter J.,Ackerman Michael J.,George Alfred L.,Wilde Arthur A.M.

Funder

National Institutes of Health

Telethon-Italy

Gilead Sciences, Inc.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference107 articles.

1. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome;Wang;Cell,1995

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

3. Positional cloning of a novel potassium channel gene: KvLQT1 mutations cause cardiac arrhythmias;Wang;Nat Genet,1996

4. The long Q-T syndrome;Schwartz;Am Heart J,1975

5. Idiopathic long QT syndrome: progress and questions;Schwartz;Am Heart J,1985

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