CALM3 mutation associated with long QT syndrome
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
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4. Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome;Boczek;Circ Cardiovasc Genet,2013
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1. Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant;HeartRhythm Case Reports;2023-12
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3. Pediatric and Familial Genetic Arrhythmia Syndromes–Evaluation of Prolonged QTc–Differential Diagnosis and what You Need to Know;Cardiac Electrophysiology Clinics;2023-11
4. JCS/JHRS 2022 Guideline on Diagnosis and Risk Assessment of Arrhythmia;Circulation Journal;2023-09-11
5. Long QT syndrome‐associated calmodulin variants disrupt the activity of the slowly activating delayed rectifier potassium channel;The Journal of Physiology;2023-07-10
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