Associated Papers
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome.
Rabbani B et al.
American Journal of Medical Genetics. Part A, 2021
Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation.
Sarquella-Brugada G et al.
Frontiers in Pediatrics, 2020
International Triadin Knockout Syndrome Registry.
Clemens DJ et al.
Circulation. Genomic and Precision Medicine, 2019
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