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Pedigree of the proband identified with MYLK3 mutations. Familial analysis was performed in the pedigree of DCM‐155. A 19‐year‐old male carrier (III‐4) showed dilation of the left ventricle on echocardiography and ST‐T abnormalities on electrocardiography, although these findings did not meet clinical criteria for DCM. All non‐carriers had the normal ventricular size on echocardiographic and also had normal electrocardiographic findings. DCM, dilated cardiomyopathy.
