Associated Papers
Whole-Exome Sequencing Identifies a Novel Variant (c.1538T > C) of TNNI3K in Arrhythmogenic Right Ventricular Cardiomyopathy.
Xie T et al.
Frontiers in Cardiovascular Medicine, 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
Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.
Liu J et al.
Journal of Clinical Laboratory Analysis, 2020
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