MYPN and familial dilated cardiomyopathy: The pathogenic variant on chr10:69959174 C > T affects one allele of the gene encoding Myopalladin (MYPN), leading to a missense mutation p.P1112L, previously reported in patients with HCM or DCM (Kimura, 2016 #5)(Duboscq-Bidot, 2008 #18).