Genetic analysis of the G4.5 gene in families with suspected Barth syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth;J Neurol Sci,1983
2. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria;Kelley;J Pediatr,1991
3. Barth Syndrome: clinical observations and genetic linkage studies;Christodoulou;Am J Hum Genet,1994
4. Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth Syndrome) to Xq28;Bolhuis;Am J Hum Genet,1991
5. Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28;Ades;Am J Med Genet,1993
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