Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test-Reference-Cited by-同舟云学术

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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test

Published:2009-09 Issue:9 Volume:6 Page:1297-1303
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Kapplinger Jamie D.,Tester David J.,Salisbury Benjamin A.,Carr Janet L.,Harris-Kerr Carole,Pollevick Guido D.,Wilde Arthur A.M.,Ackerman Michael J.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference36 articles.

1. Cardiac channelopathies: it's in the genes;Ackerman;Nat Med,2004

2. Electrocardiographic and genetic screening for long QT syndrome: results from a prospective study on 44,596 neonates (abstract 1778);Stramba-Badiale;Circulation,2007

3. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias;Wang;Nat Genet,1996

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

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

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