"Observational study of gene-disease association. (HuGE Navigator); Three heterozygous MYH6 missense mutations were identified in dilated cardiomyopathy probands (P830L A1004S and E1457K; 4.3% of probands). A Q1065H mutation was detected in 1 of 21 hypertrophic cardiomyopathy probands."xsd:string