X-linked creatine transporter deficiency results in prolonged QTc and increased sudden death risk in humans and disease model
- 28 May 2021
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 23 (10), 1864-1872
- https://doi.org/10.1038/s41436-021-01224-8
Abstract
No abstract availableThis publication has 37 references indexed in Scilit:
- Rearrangement of energetic and substrate utilization networks compensate for chronic myocardial creatine kinase deficiencyJournal Of Physiology-London, 2011
- Cardiac electrical remodeling in health and diseaseTrends in Pharmacological Sciences, 2011
- Electrophysiological remodeling in heart failureJournal of Molecular and Cellular Cardiology, 2010
- Melanocyte-like cells in the heart and pulmonary veins contribute to atrial arrhythmia triggersJCI Insight, 2009
- Creatine uptake in mouse hearts with genetically altered creatine levelsJournal of Molecular and Cellular Cardiology, 2008
- Cardiac structure and function during ageing in energetically compromised Guanidinoacetate N-methyltransferase (GAMT)-knockout mice – a one year longitudinal MRI studyJournal of Cardiovascular Magnetic Resonance, 2008
- Reduced Inotropic Reserve and Increased Susceptibility to Cardiac Ischemia/Reperfusion Injury in Phosphocreatine-Deficient Guanidinoacetate- N -Methyltransferase–Knockout MiceJournal of the American College of Cardiology, 2005
- In vivo cardiac 1H‐MRS in the mouseMagnetic Resonance in Medicine, 2004
- X-Linked Creatine-Transporter Gene (SLC6A8) Defect: A New Creatine-Deficiency SyndromeAmerican Journal of Human Genetics, 2001
- Hypertrophic cardiomyopathy with unusual locations of left ventricular hypertrophy undetectable by M-mode echocardiography. Identification by wide-angle two-dimensional echocardiography.Journal of the American College of Cardiology, 1981