Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation-Reference-Cited by-同舟云学术

Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation

Published:2005-03 Issue:5 Volume:95 Page:700-702
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Allouis Marie,Probst Vincent,Jaafar Philippe,Schott Jean-Jacques,Le Marec Hervé

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference8 articles.

1. Catecholaminergic polymorphic ventricular tachycardia in children;Leenhardt;Circulation,1995

2. Bidirectional tachycardia in a child;Reid;Br Heart J,1975

3. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia;Laitinen;Circulation,2001

4. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia;Priori;Circulation,2001

5. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2);Tiso;Hum Mol Genet,2001

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