Genetic testing in specific cardiomyopathies
Open Access
- 29 June 2009
- journal article
- Published by H1 Connect in F1000 Medicine Reports
- Vol. 1 (52)
- https://doi.org/10.3410/m1-52
Abstract
Genetic testing in specific cardiomyopathiesThis publication has 17 references indexed in Scilit:
- Contemporary Definitions and Classification of the CardiomyopathiesJournal of the American College of Cardiology, 2006
- Role of Genetic Analyses in CardiologyJournal of the American College of Cardiology, 2006
- A Novel Form of Short QT Syndrome (SQT3) Is Caused by a Mutation in the KCNJ2 GeneCirculation Research, 2005
- Mutation in the KCNQ1 Gene Leading to the Short QT-Interval SyndromeJournal of the American College of Cardiology, 2004
- Short QT syndrome: pharmacological treatmentJournal of Invasive Cardiology, 2004
- Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERGJournal of the American College of Cardiology, 2004
- Risk Stratification in the Long-QT SyndromeThe New England Journal of Medicine, 2003
- Natural history of dilated cardiomyopathy due to lamin A/C gene mutationsJournal of Invasive Cardiology, 2003
- Increased Risk of Arrhythmic Events in Long-QT Syndrome With Mutations in the Pore Region of the Human Ether-a-go-go–Related Gene Potassium ChannelJournal of the American College of Cardiology, 2002
- Clinical and Genetic Heterogeneity of Right Bundle Branch Block and ST-Segment Elevation SyndromeJournal of the American College of Cardiology, 2000