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Article

Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Nature clinical practice. Cardiovascular medicine - 1 Dec 2008

Posch Maximilian G, Posch Matthias J, Perrot Andreas, Dietz Rainer, Ozcelik Cemil

Abstract excerpt

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Topics

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Share to Arrhythmogenic Right Ventricular Dysplasia
Share to Cardiomyopathy, Dilated
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Desmoglein 2

Share to Gene Frequency

Share to Genetic Predisposition to Disease

Share to Polymorphism, Genetic

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Source

Identifiers

PMID: 19039334
DOI: 10.1038/ncpcardio1434

Genes

DSG2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Click a neighbor to travelStep 1 · 12 closest

Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy.PMID 19039334Read ↗

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.Semantic proximity Read ↗

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease.Semantic proximity Read ↗

Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2.Semantic proximity Read ↗

Natural History and Clinical Outcomes of Patients With DSG2/DSC2 Variant-Related Arrhythmogenic Right Ventricular CardiomyopathySemantic proximity Read ↗

Whole-exome sequencing identifies a novel mutation of DSG2 (Y198C) in a Chinese arrhythmogenic right ventricular cardiomyopathy patient.Semantic proximity Read ↗

Genetics of arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.Semantic proximity Read ↗

Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation databaseSemantic proximity Read ↗

Genotype–phenotype correlation in arrhythmogenic right ventricular cardiomyopathy—risk of arrhythmias and heart failureSemantic proximity Read ↗

Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes.Semantic proximity Read ↗

Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles.Semantic proximity Read ↗

DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy.Semantic proximity Read ↗

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