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Schematic representation of the filtering process of targeted capture and sequencing data from 387 HCM patients. Among the 387 HCM probands included in the study, 98 were found to carry MYH7 mutations. Among 5 probands with double MYH7 mutations, 4 probands carried compound heterozygous mutations and 1 proband carried monoallelic double mutations. MYH7, β-myosin heavy chain (MHC) 7; HCM, hypertrophic cardiomyopathy.
