Barth syndrome may be due to an acyltransferase deficiency
Author:
Publisher
Elsevier BV
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Reference13 articles.
1. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts;Barth;J Inherit Metab Dis,1996
2. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth;J Neurol Sci,1983
3. Endocardial fibroelastosis: possible X-linked inheritance;Hodgson;J Med Genet,1987
4. Possible X-linked congenital mitochondrial cardiomyopathy in three families;Orstavik;J Med Genet,1993
5. X-linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome;Gedeon;J Med Genet,1995
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