about
Mutations 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 cardiomyopathyGenetics of arrhythmogenic right ventricular cardiomyopathyUltrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsiesGenetic bases of arrhythmogenic right ventricular CardiomyopathyMissense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitroA founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of lifeMultiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasiaIdentification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathyCompound 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
@nl
researcher
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հետազոտող
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name
Alessandra Rampazzo
@ast
Alessandra Rampazzo
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Alessandra Rampazzo
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Alessandra Rampazzo
@nl
Alessandra Rampazzo
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type
label
Alessandra Rampazzo
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Alessandra Rampazzo
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Alessandra Rampazzo
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Alessandra Rampazzo
@nl
Alessandra Rampazzo
@sl
prefLabel
Alessandra Rampazzo
@ast
Alessandra Rampazzo
@en
Alessandra Rampazzo
@es
Alessandra Rampazzo
@nl
Alessandra Rampazzo
@sl