Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor function
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Title
Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor function
Authors
Keywords
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Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 112, Issue 13, Pages E1669-E1677
Publisher
Proceedings of the National Academy of Sciences
Online
2015-03-17
DOI
10.1073/pnas.1419795112
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- Heterogeneity of Ryanodine Receptor Dysfunction in a Mouse Model of Catecholaminergic Polymorphic Ventricular Tachycardia
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- Inherited calcium channelopathies in the pathophysiology of arrhythmias
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- Inherited Dysfunction of Sarcoplasmic Reticulum Ca 2+ Handling and Arrhythmogenesis
- (2011) Silvia G. Priori et al. CIRCULATION RESEARCH
- Ryanodine receptors
- (2011) E Michelle Capes et al. Skeletal Muscle
- Catecholaminergic Polymorphic Ventricular Tachycardia Is Caused by Mutation-Linked Defective Conformational Regulation of the Ryanodine Receptor
- (2010) Hitoshi Uchinoumi et al. CIRCULATION RESEARCH
- Interplay of voltage and Ca-dependent inactivation of L-type Ca current
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