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2004, ISBN 1405118385, vi, 199
Book
The New England Journal of Medicine, ISSN 0028-4793, 01/2008, Volume 358, Issue 2, pp. 169 - 176
After a 13-year-old girl dies suddenly while playing basketball, her family comes to the clinic for medical evaluation. Her parents' resting electrocardiograms... 
MEDICINE, GENERAL & INTERNAL | TORSADES-DE-POINTES | THERAPY | T-WAVE PATTERNS | GENE | FLECAINIDE | GENOTYPE | CARDIAC-ARRHYTHMIAS | RISK | MUTATIONS | POTASSIUM CHANNEL | Case studies | Long QT syndrome | Care and treatment | Diagnosis | Patient outcomes | Ventricular fibrillation | Electrocardiography | Families & family life | Cardiac arrhythmia | Postpartum period | Mutation
Journal Article
1997, Clinical approaches to tachyarrhythmias, ISBN 9780879936808, Volume 7, ix, 108
Book
Journal of the American College of Cardiology, ISSN 0735-1097, 02/2011, Volume 57, Issue 7, pp. 802 - 812
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2007, Volume 49, Issue 3, pp. 329 - 337
Journal Article
2002, Clinical approaches to tachyarrhythmias, ISBN 9780879934682, Volume 16, ix, 110
Book
Nature, ISSN 0028-0836, 03/2011, Volume 471, Issue 7337, pp. 225 - 229
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 01/2016, Volume 61, Issue 1, pp. 51 - 55
Congenital long QT syndrome (LQTS) is an inherited arrhythmia syndrome characterized by a prolonged QT interval in the 12-lead ECG, torsades de pointes and not... 
CHANNEL | DISEASE | GENETICS & HEREDITY | PHENOTYPE | CARDIAC-ARRHYTHMIA | RISK | MECHANISMS | MUTATIONS | LANGE-NIELSEN-SYNDROME | MOLECULAR-BASIS | MANIFESTATIONS | Ion Channels - genetics | Long QT Syndrome - genetics | Long QT Syndrome - diagnosis | Mutation | Humans
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2007, Volume 49, Issue 10, pp. 1092 - 1098
Journal Article