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Alström syndrome, arrhythmia, cardiomyopathy.
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cardiomyopathies, arrhythmia syndromes, splice mutations, molecular diagnosis.
cardiovascular research, bioinformatic approaches.
echocardiography, Fabry disease, cardiomyopathy.
education, cardiogenetics, endurance exercise, cardiovascular benefits.
education, familial hypertrophic cardiomyopathy phenotype, left ventricular systolic dysfunction, extensive myocardial fibrosis, cardiogenetics.
hypertrophic cardiomyopathy, HCM, gene expression, microarray.
idiopathic restrictive cardiomyopathy, hypertrophic cardiomyopathy, sarcomeric genes.
idiopathic ventricular fibrillation, cardiac arrest, gene mutation, Brugada syndrome.
inherited cardiac disease
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sequence capture, massively parallel sequencing, restrictive cardiomyopathy, desmin, missense mutation.
sudden cardiac death
Marino, Bruno, Department of Pediatrics, Pediatric Cardiology, University La Sapienza, Rome, Italy
Vol 1, No 1 (2011)
- Review Articles
Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes
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