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Molecular Insights into Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Plakophilin-2 Missense Mutations | Circulation: Cardiovascular Genetics
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Representation of PKP2 domains. A- Representation of wild type PKP2. It... | Download Scientific Diagram
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Plakophilin-2 truncating variants impair cardiac contractility by disrupting sarcomere stability and organization | Science Advances
![Schematic representation of 2 heterozygous genomic deletions of the... | Download Scientific Diagram Schematic representation of 2 heterozygous genomic deletions of the... | Download Scientific Diagram](https://www.researchgate.net/publication/320445829/figure/fig1/AS:677147161145344@1538455872543/Schematic-representation-of-2-heterozygous-genomic-deletions-of-the-plakophilin-2-PKP2.jpg)
Schematic representation of 2 heterozygous genomic deletions of the... | Download Scientific Diagram
![Characterization of the molecular phenotype of two arrhythmogenic right ventricular cardiomyopathy (ARVC)-related plakophilin-2 (PKP2) mutations - ScienceDirect Characterization of the molecular phenotype of two arrhythmogenic right ventricular cardiomyopathy (ARVC)-related plakophilin-2 (PKP2) mutations - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1547527108008771-gr3.jpg)
Characterization of the molecular phenotype of two arrhythmogenic right ventricular cardiomyopathy (ARVC)-related plakophilin-2 (PKP2) mutations - ScienceDirect
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PKP2 variant, c.1511-1G>C. (A) Genomic DNA sequence. Noted nucleotide... | Download Scientific Diagram
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Plakophilin-2 truncating variants impair cardiac contractility by disrupting sarcomere stability and organization | Science Advances
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Frontiers | Transcriptomic Coupling of PKP2 With Inflammatory and Immune Pathways Endogenous to Adult Cardiac Myocytes
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0247 : Detection and prevalence of large PKP2 deletion in arrhythmogenic right ventricular cardiomyopathy using exome sequencing, qPCR and multiplex ligation-dependent probe amplification (MLPA®) - ScienceDirect
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Genes | Free Full-Text | Clinical and Molecular Data Define a Diagnosis of Arrhythmogenic Cardiomyopathy in a Carrier of a Brugada-Syndrome-Associated PKP2 Mutation
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Loss of Nuclear Envelope Integrity and Increased Oxidant Production Cause DNA Damage in Adult Hearts Deficient in PKP2: A Molecular Substrate of ARVC | Circulation
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Clinical Features of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Associated With Mutations in Plakophilin-2 | Circulation
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Progressive Reduction in Right Ventricular Contractile Function Attributable to Altered Actin Expression in an Aging Mouse Model of Arrhythmogenic Cardiomyopathy | Circulation
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