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To cite this article: MICHEU MM, POPA-FOTEA NM, OPRESCU N, DOROBANTU M, RATIU AC, ECOVOIU A. AL., NGS data validated by Sanger sequencing reveal a puzzling small deletion of MYBPC3 gene associated with hypertrophic cardiomyopathy. Abstract Hypertrophic cardiomyopathy (HCM) has a special place among genetic cardiomyopathies, being one of the main causes of sudden death in young patients, mainly in performance athletes. Herein we report a deletion in the myosin binding protein C (MYBPC3) genedoi:10.25083/rbl/24.1/91.99 fatcat:efhll6ntyzetfh5bwc7uogquom