Associated Papers
Exploring the c.406 C > T variant in TNNI3 gene: pathogenic insights into restrictive cardiomyopathy.
Masoumi T et al.
Bmc Medical Genomics, 2025
Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.
Mehvari S et al.
Clinical Genetics, 2024
Establishment of a Dedicated Inherited Cardiomyopathy Clinic: From Challenges to Improved Patients' Outcome.
Smith E et al.
Journal of the American Heart Association, 2022
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