Dilated cardiomyopathy (DCM), usually diagnosed as idiopathic dilated cardiomyopathy
(IDC), has been shown to have a familial basis in 20–35% of cases. Genetic studies in …

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The identification of the molecular causes and subsequent insight into the molecular
mechanisms of DCM is expanding our understanding of DCM pathogenesis and highlights …

Dilated cardiomyopathy (DCM) is a myocardial disorder that is a major cause of heart failure
and death. Recent data indicate that genetic factors are important in the pathogenesis of …

Dilated cardiomyopathy (DCM) is a myocardial disorder defined by ventricular chamber
enlargement and systolic dysfunction that can result in progressive heart failure …

A great deal of progress has recently been made in the discovery and understanding of the
genetics of familial dilated cardiomyopathy (FDC). A consensus has emerged that with a …

Introduction: Dilated cardiomyopathy (DCM) is the most common cardiomyopathy and
occurs often in families. As an inherited disease, understanding the significance of …

Abstract Purpose of Review This review aims to summarize the current knowledge on the
genetic background of dilated cardiomyopathy (DCM), with particular attention to the …

Dilated cardiomyopathy (DCM) is a myocardial disease characterized by dilatation and
impaired systolic function of the left or both ventricles. The etiology of DCM is multifactorial …

Genetic mutations account for a significant percentage of cardiomyopathies, which are a
leading cause of congestive heart failure. In hypertrophic cardiomyopathy (HCM), cardiac …