General Mitochondrial Trifunctional Protein (TFP) Deficiency as a Result of Either α- or β-Subunit Mutations Exhibits Similar Phenotypes Because Mutations in Either Subunit Alter TFP Complex Expression and Subunit Turnover
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference29 articles.
1. Intact α-Subunit Is Required for Membrane Binding of Human Mitochondrial Trifunctional β-Oxidation Protein, but Is Not Necessary for Conferring 3-Ketoacyl-CoA Thiolase Activity to the β-Subunit
2. The Genes for the α and β Subunits of the Mitochondrial Trifunctional Protein Are Both Located in the Same Region of Human Chromosome 2p23
3. Biochemical Characterization and Crystal Structure Determination of Human Heart Short Chain l-3-Hydroxyacyl-CoA Dehydrogenase Provide Insights into Catalytic Mechanism
4. A Fetal Fatty-Acid Oxidation Disorder as a Cause of Liver Disease in Pregnant Women
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