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Thanks to Reviewers
Anderson-Fabry, heart failure, renal failure, stroke, genetics, enzyme replacement therapy.
Brugada syndrome, arrhythmia, genetics, double mutant, sodium channel.
European Society of Cardiology (ESC)
cardiomyopathies, arrhythmia syndromes, splice mutations, molecular diagnosis.
cardiomyopathy, sarcomere protein disease, classification, diastology.
cardiovascular research, bioinformatic approaches.
congestive heart failure
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epigenetics, cardiovascular disease, primary prevention, hypercholesterolemia, novel risk factors.
hypertrophic cardiomyopathy, HCM, gene expression, microarray.
idiopathic restrictive cardiomyopathy, hypertrophic cardiomyopathy, sarcomeric genes.
inherited cardiac disease
lysosomal storage disorders, diagnosis and management.
mucopolysaccharidoses (MPS), heart, heart and MPS, genetics and MPS.
myocardial and pericardial diseases
sequence capture, massively parallel sequencing, restrictive cardiomyopathy, desmin, missense mutation.
sudden cardiac death
β adrenergic receptor, sympathetic nervous system.
Girolami, Francesca, Genetic Diagnostics, Careggi University Hospital, Florence, Italy
Vol 1, No 1 (2011)
Genetic testing for hypertrophic cardiomyopathy: ongoing voyage from exploration to clinical exploitation
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