Article Processing Charge
Combined use of in silico and in vitro splicing...
views since: 2012-06-05
Compound heterozygous SCN5A gene mutations in...
views since: 2012-09-17
Novel SCN5A mutation associated with idiopathic...
views since: 2011-12-20
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
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
β adrenergic receptor, sympathetic nervous system.
Algarra, Maria, Cardiology Department, Virgen de las Nieves Universitary Hospital, Granada, Spain
Vol 2, No 1 (2012)
- Original Articles
Novel SCN5A mutation associated with idiopathic ventricular fibrillation due to subclinical Brugada syndrome
[eISSN 2035-8148] is a new Open Access, online-only, peer-reviewed journal published by
, Pavia, Italy. All credits and honors to
© PAGEPress 2008-2015 -
is a registered trademark property of PAGEPress srl, Italy. - VAT: IT02125780185