The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies
- 1 October 1997
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 61 (4), 862-867
- https://doi.org/10.1086/514886
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Molecular Genetic Insights into Cardiovascular DiseaseScience, 1996
- A novel X-linked gene, G4.5. is responsible for Barth syndromeNature Genetics, 1996
- When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.1995
- X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.Journal of Medical Genetics, 1995
- Barth syndrome: Clinical observations and genetic linkage studiesAmerican Journal of Medical Genetics, 1994
- Possible X linked congenital mitochondrial cardiomyopathy in three families.Journal of Medical Genetics, 1993
- Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28American Journal of Medical Genetics, 1993
- X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduriaThe Journal of Pediatrics, 1991
- An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytesJournal of the Neurological Sciences, 1983
- Two cases of endocardial fibroelastosis--possible x-linked determination.Heart, 1973