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Cellular Physiology and Biochemistry, ISSN 1015-8987, 10/2017, Volume 42, Issue 5, pp. 2021 - 2029
Journal Article
Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 4, pp. 316 - 320
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 2014, Volume 64, Issue 8, pp. 745 - 756
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2014, Volume 64, Issue 8, pp. 757 - 767
Abstract Background Inherited arrhythmias were originally considered isolated electrical defects. There is growing evidence that ion channel dysfunction also... 
Cardiovascular | Internal Medicine | HCN4 | noncompaction cardiomyopathy | overlap syndrome | sinus node dysfunction | sinus node dysfunction | ACTIVATION | CARDIAC & CARDIOVASCULAR SYSTEMS | MUSCLE LIM PROTEIN | DILATED CARDIOMYOPATHY | BRADYCARDIA | LEFT-VENTRICULAR NONCOMPACTION | HYPERTROPHIC CARDIOMYOPATHY | NON-COMPACTION | CONDUCTION | HUMAN HEART | PACEMAKER CHANNEL | Prevalence | Humans | Middle Aged | Male | Sick Sinus Syndrome - diagnostic imaging | Young Adult | Heart Defects, Congenital - genetics | Heart Defects, Congenital - diagnostic imaging | HEK293 Cells | Female | Sick Sinus Syndrome - genetics | Sick Sinus Syndrome - epidemiology | Echocardiography | Syndrome | Germany - epidemiology | Potassium Channels - genetics | Muscle Proteins - genetics | Phenotype | Animals | Membrane Potentials | Pedigree | Adolescent | Heart Defects, Congenital - epidemiology | Electrophysiologic Techniques, Cardiac | Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels - genetics | Physiological aspects | Genetic aspects | Arrhythmia | Neurophysiology | Heart failure | Cardiac arrhythmia | Cardiomyopathy | Genes | Cardiovascular disease | Patients | Studies | Heart rate | Genotype & phenotype | Sinuses | Mutagenesis | Electrocardiography | Software | Mutation | Genetic testing | Deoxyribonucleic acid--DNA | Methods
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2010, Volume 42, Issue 2, pp. 117 - 122
Electrocardiographic measures are indicative of the function of the cardiac conduction system. To search for sequence variants that modulate heart rate, PR... 
ALPHA-MYOSIN | DISEASE | GENETICS & HEREDITY | HOLT-ORAM-SYNDROME | SODIUM-CHANNEL | ISCHEMIC-STROKE | EXPRESSION | MYOSIN HEAVY-CHAIN | GENOME-WIDE ASSOCIATION | ATRIAL-FIBRILLATION | GENETIC-FACTORS | Atrioventricular Block - genetics | Humans | Middle Aged | Genetic Loci - genetics | Myosin Heavy Chains - genetics | Male | Atrial Fibrillation - physiopathology | Arrhythmias, Cardiac - physiopathology | Iceland | Pacemaker, Artificial | Genetic Variation | Heart Conduction System - physiology | Electrocardiography | Inheritance Patterns - genetics | Atrioventricular Block - complications | Female | Sick Sinus Syndrome - genetics | Arrhythmias, Cardiac - genetics | Atrioventricular Block - physiopathology | Genome-Wide Association Study | Reproducibility of Results | Sick Sinus Syndrome - complications | Cardiac Myosins - genetics | Heart Rate - genetics | Atrial Fibrillation - complications | Atrial Fibrillation - genetics | Sick Sinus Syndrome - physiopathology | Aged | Arrhythmias, Cardiac - complications | Measurement | Usage | Care and treatment | Heart beat | Electrocardiogram | Atrial fibrillation | Physiological aspects | Genetic aspects | Research | Diagnosis | Health aspects | Heart rate | Studies | Cardiac arrhythmia | Heart attacks | Mortality | Nitric oxide | Data collection | Cardiovascular disease | Gene expression | Risk factors
Journal Article
Journal Article
Heart Rhythm, ISSN 1547-5271, 2014, Volume 11, Issue 6, pp. 1015 - 1023
Journal Article
Journal Article
Circulation Research, ISSN 0009-7330, 07/2017, Volume 121, Issue 5, pp. 549 - 563
Journal Article