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Article

Molecular insights into cardiomyopathies associated with desmin (DES) mutations

20 Jun 2018

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 29926427
DOI: 10.1007/s12551-018-0429-0

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Molecular insights into cardiomyopathies associated with desmin (DES) mutationsPMID 29926427Read ↗

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Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death.Semantic proximity Read ↗

High Burden of Ventricular Arrhythmias and Cardiac Conduction Disease in Pediatric Patients with Pathogenic Desmin (<i>DES</i>) VariantsSemantic proximity Read ↗

Desmin p.R406W mutation is associated with arrhythmias through structural and electrophysiological remodelingSemantic proximity Read ↗

Heterozygous desmin gene (DES) mutation contributes to familial dilated cardiomyopathy.Semantic proximity Read ↗

High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.Semantic proximity Read ↗

Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutationSemantic proximity Read ↗

Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes.Semantic proximity Read ↗

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