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Article

New insight into the variable expression of arrhythmogenic right ventricular cardiomyopathy provided by the analysis of a plakophilin-2 splice mutation.

Cardiology - 1 Jan 2012

Gandjbakhch E, Charron P

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Share to Arrhythmogenic Right Ventricular Dysplasia
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PMID: 23183494
DOI: 10.1159/000345293

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Related research

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New insight into the variable expression of arrhythmogenic right ventricular cardiomyopathy provided by the analysis of a plakophilin-2 splice mutation.PMID 23183494Read ↗

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family.Semantic proximity Read ↗

A Novel Mutation of the Plakophilin-2 Gene in a Child with Early Onset Arrhythmogenic Right Ventricular Cardiomyopathy and Intractable Arrhythmia.Semantic proximity Read ↗

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Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy.Semantic proximity Read ↗

Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation.Semantic proximity Read ↗

Arrhythmogenic Cardiomyopathy: Towards Genotype Based Diagnoses and ManagementSemantic proximity Read ↗

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

Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Plakophilin-2 missense mutations in arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Genetics of arrhythmogenic right ventricular cardiomyopathy.Semantic proximity Read ↗

Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense MutationsSemantic proximity Read ↗

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