A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardia
Authors:
- 1 March 2005
- journal article
- research article
- Published by Elsevier in International Journal of Cardiology
- Vol. 99 (2) , 343-345
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular TachycardiaCirculation, 2001
- Arrhythmic disorder mapped to chromosome 1q42–q43 causes malignant polymorphic ventricular tachycardia in structurally normal heartsJACC, 1999