Arrhythmogenic Cardiomyopathy (ACM), a Mendelian disorder that can affect both left and
right ventricles, is most often associated with pathogenic desmosomal variants that can lead …

Arrhythmogenic cardiomyopathy (ACM) is a heritable heart muscle disease associated with
increased risk of sudden cardiac death. The only treatment proven to reduce this risk is an …

Arrhythmogenic cardiomyopathy (ACM) is a rare, heritable heart disease characterized by
fibro-fatty replacement of the myocardium and a high degree of electric instability. It was first …

Arrhythmogenic cardiomyopathy (ACM) is an inherited disorder characterized by structural
and electrical cardiac abnormalities, including myocardial fibro-fatty replacement. Its …

Arrhythmogenic cardiomyopathy (ACM) is a heritable myocardial disease that manifests with
cardiac arrhythmias, syncope, sudden cardiac death, and heart failure in the advanced …

Arrhythmogenic cardiomyopathy (AC) is a hereditary cardiac disorder characterized by the
gradual replacement of cardiomyocytes with fibrous and adipose tissue, leading to …

Background Both gap junctional remodeling and interstitial fibrosis have been linked to
impaired electrical conduction velocity (CV) and fatal ventricular arrhythmias in nonischemic …

Gap junction and ion channel remodeling occur early in Arrhythmogenic Cardiomyopathy
(ACM), but their pathogenic consequences have not been elucidated. Here, we identified …

Arrhythmogenic cardiomyopathy (AC) is a clinically and genetically heterogeneous disorder
of heart muscle that is associated with ventricular arrhythmias and risk of sudden cardiac …

Arrhythmogenic cardiomyopathy (ACM) is characterized by frequent cardiac arrhythmias. To
elucidate the underlying mechanisms and discover potential chemical modifiers, we created …