Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy
- 17 December 2001
- journal article
- case report
- Published by Wolters Kluwer Health in Circulation
- Vol. 104 (25) , 3030-3033
- https://doi.org/10.1161/hc5001.102111
Abstract
Background— We recently reported a mutation in the PRKAG2 gene to be responsible for a familial syndrome of ventricular preexcitation, atrial fibrillation, conduction defects, and cardiac hypertrop...Keywords
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