Varaico: Literature-Extracted Genetic Variants

Gene:TRDN
Variant:p.K206delFs
Back to variants list

TRDN

NM_006073.4:p.K206delFs

Associated Papers

Unusual catecholaminergic polymorphic ventricular tachycardia and bradycardia caused by a novel triadin variant in 2 siblings from a Malian family.

Diakité M et al.

Medicine, 2025

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

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."