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

Abstract Purpose of Review Dilated cardiomyopathy (DCM) is characterized by left
ventricular dilation and systolic function and is the most common among all …

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 defined as dilation and/or reduced function of one or both
ventricles and remains a common disease worldwide. An estimated 40% of cases of familial …

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 disease transmission has been identified in a significant proportion of patients with
dilated cardiomyopathy (DCM). Variable clinical characteristics and patterns of inheritance …

Dilated cardiomyopathy (DCM) is a common and important cause of morbidity and mortality.
Many factors can contribute to the development of this disorder, although most commonly …

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