Associated Papers
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data sets.
Butters A et al.
European Heart Journal, 2025
Genetic Screening Reveals Heterogeneous Clinical Phenotypes in Patients with Dilated Cardiomyopathy and Troponin T2 Variants.
Weis A et al.
Journal of Personalized Medicine, 2023
37108997 (PubMed )
Supplement: jpm-13-00611-s001.zip › jpm-2274209-supplementary.pdf
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