Alert me about new articles
Thanks to Reviewers
Alström syndrome, arrhythmia, cardiomyopathy.
Brugada syndrome, arrhythmia, genetics, double mutant, sodium channel.
atrium, cardiac surgery, haematopoietic progenitor cells, myxoma, trisomy.
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
mitochondrial DNA, respiratory chain deficiency, mitochondrial cardiomyopathy, T3258C, A3243G.
sequence capture, massively parallel sequencing, restrictive cardiomyopathy, desmin, missense mutation.
sudden cardiac death
Clauss, Sebastian, Department of Medicine I, University Hospital Munich, Campus Grosshadern, Ludwig- Maximilians University, Munich, Germany
Vol 1, No 1S (2011): Ion channel diseases: molecular basis, clinical findings, and management
- Review Articles
Recent advances in the genetics of atrial fibrillation: from rare and common genetic variants to microRNA signaling
[eISSN 2035-8148] is a new Open Access, online-only, peer-reviewed journal published by PAGEPress
, Pavia, Italy. All credits and honors to
© PAGEPress 2008-2014 -
is a registered trademark property of PAGEPress srl, Italy. - VAT: IT02125780185