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Article

Mutation in Human Desmoplakin Domain Binding to Plakoglobin Causes a Dominant Form of Arrhythmogenic Right Ventricular Cardiomyopathy

1 Nov 2002

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12373648
DOI: 10.1086/344208

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation in Human Desmoplakin Domain Binding to Plakoglobin Causes a Dominant Form of Arrhythmogenic Right Ventricular CardiomyopathyPMID 12373648Read ↗

Arrhythmogenic Right Ventricular Cardiomyopathy Caused by a Deletion in Plakoglobin (Naxos Disease)Semantic proximity Read ↗

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Arrhythmogenic right ventricular dysplasia, a cell adhesion cardiomyopathy: insights into disease pathogenesis from preliminary genotype—phenotype assessment: Figure 1Semantic proximity Read ↗

A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype.Semantic proximity Read ↗

A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hairSemantic proximity Read ↗

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

Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy.Semantic proximity Read ↗

A mutation in the Z‐line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathySemantic proximity Read ↗

Left-Dominant Arrhythmogenic Cardiomyopathy, Palmoplantar Keratoderma, and Curly Hair Associated With a Rare Autosomal Dominant Truncating Variant in Desmoplakin.Semantic proximity Read ↗

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).Semantic proximity Read ↗

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathySemantic proximity Read ↗

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