Una nueva mutación en el gen del receptor de la rianodina (RyR2 C2277R) como causa de taquicardia ventricular polimórfica catecolaminérgica
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
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2. The Role of Ca2+-ATPase 2a (ATP2A2), Ryanodine Receptors (RYR2), and Calsequestrin (CASQ2) Gene Polymorphisms in the Development of Heart Failure;Russian Journal of Genetics;2018-06
3. RyR2R420Q catecholaminergic polymorphic ventricular tachycardia mutation induces bradycardia by disturbing the coupled clock pacemaker mechanism;JCI Insight;2017-04-20
4. Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications;Forensic Science, Medicine, and Pathology;2017-04-13
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