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Pathogenic Intronic Splice-Affecting Variants in MYBPC3 in Three Patients with Hypertrophic Cardiomyopathy
Mosaic Fabry Disease in a Male Presenting as Hypertrophic Cardiomyopathy
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Cardiac Amyloidosis Therapy: A Systematic Review
Three Myocardial Diseases in One Heart: Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Noncompaction and Myocarditis
The Multi-Ethnic New Zealand Study of Acute Coronary Syndromes (MENZACS): Design and Methodology
Reassessment of Gene-Elusive Familial Dilated Cardiomyopathy Leading to the Discovery of a Homozygous AARS2 Variant—The Importance of Regular Reassessment of Genetic Findings
Evaluation of the Correlation between the rs4918 Polymorphism of AHSG Gene and Coronary Artery Calcification in Patients with Coronary Artery Disease
Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report
Publisher’s Note: Continued Publication of Cardiogenetics by MDPI
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Cardiac Amyloidosis Therapy: A Systematic Review
Cardiogenetics: An Open Access Journal
Genetic Susceptibility to SARS-CoV-2: From the Nehandertal Age to 2020
Mosaic Fabry Disease in a Male Presenting as Hypertrophic Cardiomyopathy
Cardiac Involvement in Autosomal Dominant Polycystic Kidney Disease
Three Myocardial Diseases in One Heart: Arrhythmogenic Right Ventricular Cardiomyopathy, Left Ventricular Noncompaction and Myocarditis
Anomalous Left Coronary Artery from the Pulmonary Artery: The Role of Multimodal Imaging—A Case Report
Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report
Gene Therapy in Anderson-Fabry Disease. State of the Art and Future Perspectives
Pathogenic Intronic Splice-Affecting Variants in MYBPC3 in Three Patients with Hypertrophic Cardiomyopathy
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