X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

A number of families with X linked dilated cardiomyopathy with onset in infancy or childhood have now been described, with varying clinical and biochemical features. Of these, one condition, Barth syndrome (BTHS), can be diagnosed clinically by the characteristic associated features of skeletal myop...

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Bibliographic Details
Main Authors: Gedeon, A K, Wilson, M J, Colley, A C, Sillence, D O, Mulley, J C
Format: Artigo
Language:Inglês
Published: 1995
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050435/
https://ncbi.nlm.nih.gov/pubmed/7616547
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