Titin Mutations as the Molecular Basis for Dilated Cardiomyopathy
- 1 February 2002
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 291 (2) , 385-393
- https://doi.org/10.1006/bbrc.2002.6448
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Mutations in Sarcomere Protein Genes as a Cause of Dilated CardiomyopathyNew England Journal of Medicine, 2000
- Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratodermaHuman Molecular Genetics, 2000
- Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathyJournal of Clinical Investigation, 2000
- Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)The Lancet, 2000
- Desmin Mutation Responsible for Idiopathic Dilated CardiomyopathyCirculation, 1999
- Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart FailureScience, 1998
- Carnitine palmitoyltransferase in patients with cardiac ischemia due to atherosclerotic coronary artery disease and in patients with idiopathic dilated cardiomyopathy.Cardiology, 1997
- A novel X-linked gene, G4.5. is responsible for Barth syndromeNature Genetics, 1996
- Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated CardiomyopathyNew England Journal of Medicine, 1993
- The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated CardiomyopathyNew England Journal of Medicine, 1992