Associated Papers
Multifocal Atrial Tachycardia and Genetic Background-Guided Ablation Strategy for Atrial Fibrillation in a Young Woman.
Kong LC et al.
Jacc. Case Reports, 2026
Clockwise bundle branch re-entrant ventricular tachycardia in a teenage patient as the first manifestation of dilated cardiomyopathy associated with the p.Ile512Leu TNNI3k variant: a case report.
González-Quijano M et al.
European Heart Journal. Case Reports, 2025
Phenotypic expression of rare progressive cardiac conduction disease variants in the general population.
Shah RA et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology, 2025
[Dilated cardiomyopathy and conduction disorder due to TNNI3K mutation].
Gayán-Ordás J et al.
Archivos De Cardiologia De Mexico, 2025
A New Mechanism of Supraventricular Tachycardia: Gene Mutation.
Gao J et al.
Current Cardiology Reviews, 2025
Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review.
Micolonghi C et al.
International Journal of Molecular Sciences, 2024
Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia.
Pham C et al.
Clinical Genetics, 2024
Unexpected Genetic Twists in Patients with Cardiac Devices.
Goanta EV et al.
Journal of Clinical Medicine, 2024
Expression Levels of the Tnni3k Gene in the Heart Are Highly Associated with Cardiac and Glucose Metabolism-Related Phenotypes and Functional Pathways.
Gu Q et al.
International Journal of Molecular Sciences, 2023
Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias.
Pham C et al.
Circulation. Genomic and Precision Medicine, 2023
Importance of genetic testing in unexplained cardiac arrest.
Grondin S et al.
European Heart Journal, 2022
A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family.
Ramzan S et al.
Genes, 2021
The Diverse Roles of TNNI3K in Cardiac Disease and Potential for Treatment.
Pham C et al.
International Journal of Molecular Sciences, 2021
A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes.
Touat-Hamici Z et al.
Scientific Reports, 2021
The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice.
Gan P et al.
Human Molecular Genetics, 2021
Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.
Liu J et al.
Journal of Clinical Laboratory Analysis, 2020
Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency.
Gan P et al.
Plos Genetics, 2019
Molecular and genetic insights into progressive cardiac conduction disease.
Asatryan B et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology, 2019
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys).
Podliesna S et al.
Heart Rhythm, 2019
Nonsynonymous TNNI3K mutations and phenotypes: More than a "simple" cardiomyopathy.
Dittmann S et al.
Heart Rhythm, 2019