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THE MYH7, MYBPC3 GENE MUTATIONS IN HYPERTROPHIC CARDIOMYOPATHY PATIENTS RESIDING IN THE REPUBLIC OF BELARUS

Niyazova S.S., Chakova N.N., Mikhalenko A.P., Chebotareva N.V., Komissarova S.M., Krupnova E.V.

Introduction. Hypertrophic cardiomyopathy (HCM) is a common genetically heterogeneous disease caused by mutations in genes encoding proteins of the cardiac sarcomere. Mutations in the genes encoding β-myosin heavy chain (MYH7) and myosin binding protein C (MYB…