Cost-Effectiveness of Genetic Testing in Family Members of Patients With Long-QT Syndrome
Author:
Affiliation:
1. From the Stanford University School of Medicine (M.V.P., N.A.K., P.J.W., M.A.H.), Stanford, Calif; and VA Palo Alto Health Care System (D.K.O.), Palo Alto, Calif.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Reference53 articles.
1. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
2. Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
3. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death
4. MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia
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