A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding
- 1 April 2013
- journal article
- case report
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Vol. 1833 (4), 833-839
- https://doi.org/10.1016/j.bbamcr.2012.11.003
Abstract
No abstract availableKeywords
Funding Information
- Netherlands Heart Foundation (96.006)
- European Community's Sixth Framework Programme (LSHM-CT-2005-018630)
This publication has 34 references indexed in Scilit:
- Truncations of Titin Causing Dilated CardiomyopathyNew England Journal of Medicine, 2012
- Mutations in fast skeletal troponin I, troponin T, and β‐tropomyosin that cause distal arthrogryposis all increase contractile functionThe FASEB Journal, 2006
- An Atomic Model of the Thin Filament in the Relaxed and Ca2+-Activated StatesJournal of Molecular Biology, 2006
- easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analysesBioinformatics, 2004
- Clinical Characterization of Left Ventricular Noncompaction in ChildrenCirculation, 2003
- Merlin—rapid analysis of dense genetic maps using sparse gene flow treesNature Genetics, 2001
- CARDIOMYOPATHY: Diagnosis and management of dilated cardiomyopathyHeart, 2000
- Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System DiseaseNew England Journal of Medicine, 1999
- Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin GeneJournal of the American College of Cardiology, 1997
- Frequency of familial nature of dilated cardiomyopathy and usefulness of cardiac transplantation in this subsetThe American Journal of Cardiology, 1989