Associated Papers
Novel Double MYH7/MYBPC3 Variants in a Chinese Family of Hypertrophic Cardiomyopathy with Early-Onset and Sudden Death.
Wang B et al.
Cardiology, 2025
MYH7 in cardiomyopathy and skeletal muscle myopathy.
Gao Y et al.
Molecular and Cellular Biochemistry, 2024
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
Barbosa P et al.
Frontiers in Cardiovascular Medicine, 2022
36061567 (PubMed )
Supplement: Table_1.XLSX › Table_S1
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