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Brugada syndrome, arrhythmia, genetics, double mutant, sodium channel.
European Society of Cardiology (ESC)
RASopathies, hypertrophic cardiomyopathy, echocardiography.
atrium, cardiac surgery, haematopoietic progenitor cells, myxoma, trisomy.
cardiomyopathies, arrhythmia syndromes, splice mutations, molecular diagnosis.
cardiomyopathy, sarcomere protein disease, classification, diastology.
cardiovascular research, bioinformatic approaches.
congestive heart failure
education, familial hypertrophic cardiomyopathy phenotype, left ventricular systolic dysfunction, extensive myocardial fibrosis, cardiogenetics.
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
Makielski, Jonathan C., Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin, Madison, WI, United States
Vol 1, No 1 (2011)
- Original Articles
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype
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