Associated Papers
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
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
Select a paper to view details