Welcome to the Dilated Cardiomyopathy Research Project. Our goal is to advance our understanding of the genetics of dilated cardiomyopathy (DCM).
gov; Unique identifier: NCT03037632.
Background: Each of the cardiomyopathies, classically categorized as hypertrophic cardiomyopathy, dilated cardiomyopathy (DCM), and arrhythmogenic right ventricular cardiomyopathy, has a signature...
First-degree relatives of Black patients and those of patients diagnosed before age 34 were at particularly high risk.