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Arrhythmogenic right ventricular cardiomyopathy/dysplasiaMutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathyMutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathyMutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathyConsensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association For European Cardiovascular Pathology: II. Noninflammatory degenerative diseases - nomenclature and diagnostic criteriaArrhythmogenic cardiomyopathyTreatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statementTreatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus StatementConsensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology: I. Inflammatory diseasesUltrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsiesArrhythmogenic right ventricular cardiomyopathy causing sudden cardiac death in boxer dogs: a new animal model of human diseaseMissense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitroThe ARVD/C genetic variants database: 2014 updateA founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of lifeIntercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changesMultiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasiaIdentification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathyA novel kind of tumor type-characteristic junction: plakophilin-2 as a major protein of adherens junctions in cardiac myxomataCompound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy
P50
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P50
description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
@hy
name
Cristina Basso
@ast
Cristina Basso
@en
Cristina Basso
@es
Cristina Basso
@nl
Cristina Basso
@sl
type
label
Cristina Basso
@ast
Cristina Basso
@en
Cristina Basso
@es
Cristina Basso
@nl
Cristina Basso
@sl
prefLabel
Cristina Basso
@ast
Cristina Basso
@en
Cristina Basso
@es
Cristina Basso
@nl
Cristina Basso
@sl