Biochemical and Biophysical Research Communications
Volume 188, Issue 3, 16 November 1992, Pages 1139-1145
Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation
References (19)
- et al.
Biochim. Biophys. Acta
(1991) - et al.
Lancet
(1989) - et al.
Biochem. Biophys. Res. Commun
(1992) - et al.
J. Biol. Chem
(1992) - et al.
Anal. Biochem
(1990) - et al.
J. Biol. Chem
(1987) Biochim. Biophys. Acta
(1991)- et al.
Ann. Rev. Biochem
(1992) Ann. Clin. Biochem
(1990)
There are more references available in the full text version of this article.
Cited by (154)
Biochemical assays of TCA cycle and β-oxidation metabolites
2020, Methods in Cell BiologyInborn Errors of Metabolism with Myopathy: Defects of Fatty Acid Oxidation and the Carnitine Shuttle System
2018, Pediatric Clinics of North AmericaRegulation of mitochondrial trifunctional protein modulates nonalcoholic fatty liver disease in mice
2018, Journal of Lipid ResearchIdentification of enzymes involved in oxidation of phenylbutyrate
2017, Journal of Lipid ResearchNonmitochondrial Metabolic Cardioskeletal Myopathies
2017, Cardioskeletal Myopathies in Children and Young AdultsImportant mitochondrial proteins in human omental adipose tissue show reduced expression in obesity
2015, Journal of Proteomics
Copyright © 1992 Published by Elsevier Inc.