Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation
- 1 November 1992
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 188 (3) , 1139-1145
- https://doi.org/10.1016/0006-291x(92)91350-y
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- BIOCHEMISTRY OF PEROXISOMESAnnual Review of Biochemistry, 1992
- Metabolic aspects of peroxisomal β-oxidationBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1991
- Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyThe Journal of Pediatrics, 1991
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase DeficiencyPediatric Research, 1991
- 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentEuropean Journal of Pediatrics, 1991
- Beta oxidation of fatty acidsBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1991
- Deficiency of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase: A Cause of Lethal Myopathy and Cardiomyopathy in Early ChildhoodPediatric Research, 1990
- The Laboratory Diagnosis of Inborn Errors of Mitochondrial Fatty Acid OxidationAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1990
- SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASEThe Lancet, 1989
- The inborn errors of peroxisomal β‐oxidation: A reviewJournal of Inherited Metabolic Disease, 1989