Only One Splice Variant of the Human TAZ Gene Encodes a Functional Protein with a Role in Cardiolipin Metabolism
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference28 articles.
1. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)
2. X Chromosome Inactivation in Carriers of Barth Syndrome
3. Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome
4. A novel X-linked gene, G4.5. is responsible for Barth syndrome
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