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Nature Genetics, ISSN 1061-4036, 2011, Volume 43, Issue 2, pp. 121 - 126
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2019, Volume 27, pp. 1341 - 1350
Journal Article
Netherlands Heart Journal, ISSN 1568-5888, 2007, Volume 15, Issue 5, pp. 184 - 190
Journal Article
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation, ISSN 1568-5888, 05/2007, Volume 15, Issue 5, pp. 184 - 190
Hypertrophic cardiomyopathy (HCM) is a disease characterised by unexplained left ventricular hypertrophy (LVH) (i.e. LVH in the absence of another cardiac or... 
hypertrophic cardiomyopathy | genetics | Review
Journal Article
Genetic Counseling, ISSN 1015-8146, 2004, Volume 15, Issue 3, pp. 329 - 333
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 08/2014, Volume 64, Issue 8, p. 745
  Background Familial forms of primary sinus bradycardia have sometimes been attributed to mutations inHCN4,SCN5A, andANK2. In these studies, no structural... 
Cardiac arrhythmia | Genomics | Genes | Electrocardiography | Mutation
Journal Article
European Heart Journal, ISSN 0195-668X, 10/2007, Volume 28, Issue 22, pp. 2732 - 2737
  Cardiomyopathies are classified according to distinct morphological characteristics. They occur relatively frequent and are an important cause of mortality... 
Journal Article
2011, ISBN 9781849964708
Noncompaction of the left ventricle or noncompaction cardiomyopathy (NCCM) is a relatively new clinicopathologic entity, first described by Feldt et al. 
Human Genetics | Internal Medicine | Medicine & Public Health | Cardiology
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