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Article

Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutation

7 Aug 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16890305
DOI: 10.1016/j.ijcard.2006.05.019

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Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutationPMID 16890305Read ↗

Restrictive cardiomyopathy due to novel desmin gene mutation.Semantic proximity Read ↗

Molecular insights into cardiomyopathies associated with desmin (DES) mutationsSemantic proximity Read ↗

Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7 is caused by a DES mutationSemantic proximity Read ↗

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Discovery of a new mutation in the desmin gene in a young patient with cardiomyopathy and muscular weakness.Semantic proximity Read ↗

Desmin accumulation restrictive cardiomyopathy and atrioventricular block associated with desmin gene defects.Semantic proximity Read ↗

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

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly DefectSemantic proximity Read ↗

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Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy.Semantic proximity Read ↗

Deletion in TNNI3 gene is associated with restrictive cardiomyopathy.Semantic proximity Read ↗

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 ↗

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