Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference13 articles.
1. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)
2. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)—MIM 302060
3. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria
4. A novel X-linked gene, G4.5. is responsible for Barth syndrome
5. The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies
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