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
Long-Term Follow-Up of Idiopathic Ventricular Fibrillation in a Pediatric Population: Clinical Characteristics, Management, and Complications.
Frontera A et al.
Journal of the American Heart Association, 2019
International Triadin Knockout Syndrome Registry.
Clemens DJ et al.
Circulation. Genomic and Precision Medicine, 2019
Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two Siblings.
Walsh MA et al.
Pacing and Clinical Electrophysiology : Pace, 2016
Select a paper to view details