A recent study explores the role of DES (p.Leu88Met) and MYH7 (p.Arg787His) variants in familial restrictive cardiomyopathy. These findings may enhance understanding of genetic contributions to this rare heart condition.
potential contribution of des p leu88met and myh7 p arg787his variants to familial restrictive cardiomyopathy
Original title: “Potential Contribution of DES (p.Leu88Met) and MYH7 (p.Arg787His) Variants to Familial Restrictive Cardiomyopathy.”