BMP10 and familial dilated cardiomyopathy: By WES and bioinformatical analysis in the pedigree members, a heterozygous BMP10 variation, namely, NM_014482.3: c.166C > T;p.(Gln56*), was found and validated through a Sanger sequencing assay to be in co-segregation with the DCM phenotype in the whole pedigree.