The Enzymatic Function of Tafazzin
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference32 articles.
1. A novel X-linked gene, G4.5. is responsible for Barth syndrome
2. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)
3. Barth syndrome may be due to an acyltransferase deficiency
4. Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome
5. Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome
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