Associated Papers
Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes.
Clemens DJ et al.
Stem Cell Reports, 2023
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population.
Clemens DJ et al.
Circulation. Genomic and Precision Medicine, 2020
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
Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.
Altmann HM et al.
Circulation, 2015
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