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Alström syndrome, arrhythmia, cardiomyopathy.
European Society of Cardiology (ESC)
LMNA, Lamin A/C, dilated cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy.
atrium, cardiac surgery, haematopoietic progenitor cells, myxoma, trisomy.
cardiomyopathies, arrhythmia syndromes, splice mutations, molecular diagnosis.
congestive heart failure
cost-effectiveness, genetic study, cardiomyopathies, channelopathies.
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
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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