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EUROPEAN HEART JOURNAL, ISSN 0195-668X, 02/2011, Volume 32, Issue 4, pp. 390 - 392
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 03/2018, Volume 71, Issue 11, pp. 1215 - 1216
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 12/2017, Volume 70, Issue 24, pp. 3016 - 3017
Journal Article
European Heart Journal, ISSN 0195-668X, 10/2019, Volume 40, Issue 37, pp. 3108 - 3109
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 12/2017, Volume 70, Issue 24, pp. 3016 - 3017
Journal Article
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 07/2013, Volume 34, Issue 7, pp. 961 - 966
Brugada Syndrome (BrS) is a familial disease associated with sudden cardiac death. A 20%-25% of BrS patients carry genetic defects that cause loss-of-function... 
FIBRILLATION | AUXILIARY SUBUNIT | VARIANTS | ALPHA | BETA-SUBUNITS | sudden cardiac death | PATHOPHYSIOLOGY | NA(V)1.5 | QT-SYNDROME | GENETICS & HEREDITY | SCN5A | RAT-BRAIN | Brugada Syndrome | SCN2B | CHANNELOPATHIES | Heart | Genetic aspects | Glycine | Genes | Analysis | Sodium | Mutation
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2008, Volume 52, Issue 19, pp. 1567 - 1573
Journal Article
Journal Article
Circulation: Arrhythmia and Electrophysiology, ISSN 1941-3149, 11/2016, Volume 9, Issue 11
Journal Article
1987, ISBN 0879933062, xxi, 823 p., [2] leaves of plates
Book
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, p. e0133037
Background The use of next-generation sequencing enables a rapid analysis of many genes associated with sudden cardiac death in diseases like Brugada Syndrome.... 
NA(V)1.5 | ANKYRIN-G | COMMON POLYMORPHISM | MULTIDISCIPLINARY SCIENCES | COMPOUND | SUDDEN CARDIAC DEATH | PHENOTYPE | NOISE | LONG-QT SYNDROME | MUTATIONS | RIGHT-VENTRICULAR CARDIOMYOPATHY/DYSPLASIA | Brugada Syndrome - genetics | Brugada Syndrome - diagnosis | Genetic Testing | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Male | Calsequestrin - genetics | Death, Sudden, Cardiac | Genetic Variation | A Kinase Anchor Proteins - genetics | gamma Catenin | Desmoplakins - genetics | Clinical Decision-Making | Adult | Female | Retrospective Studies | NAV1.5 Voltage-Gated Sodium Channel - genetics | Arrhythmias, Cardiac - genetics | Desmoglein 2 - genetics | Penetrance | Potassium Channels, Inwardly Rectifying - genetics | Sequence Analysis, DNA | Ryanodine Receptor Calcium Release Channel - genetics | Pedigree | Ankyrins - genetics | High-Throughput Nucleotide Sequencing | Cohort Studies | Cardiac arrhythmia | Copy number | Genes | Insertion | Ryanodine receptors | Genetic screening | Gene sequencing | Complexity | Proteins | Clonal deletion | Defibrillators | Genetic analysis | Electrocardiography | Potassium channels (voltage-gated) | Heart diseases | Ion channels (cyclic nucleotide-gated) | Potassium channels (inwardly-rectifying) | Decision making | Data processing | Genetic diversity | Patients | Coronary artery disease | Substrates | Diseases | Genetic variance | KCNQ1 protein | Mutation | Variation | Malalties | Heart | Aspectes genètics | Arítmia | Arrhythmia | Cor | Genetic aspects
Journal Article
Circulation: Arrhythmia and Electrophysiology, ISSN 1941-3149, 11/2016, Volume 9, Issue 11
Journal Article
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