This is a preview of subscription content, log in via an institution to check access.
References
Carpenter K, Pollitt RJ, Middleton B (1992) Human liver long-chain 3-hydroxyacyl-coenzyme a dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria.Biochem Biophys Res Commun 183: 443–448.
Hagenfeldt L, von Döbeln U, Holme E et al (1990) 3-Hydroxydicarboxylic aciduria — a fatty acid oxidation defect with severe prognosis.J Pediatr 116: 387–392.
Kamijo T, Wanders RJA, Saudubray J-M et al (1994) Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme.J Clin Invest 93: 1740–1747.
Pollitt RJ, Losty H, Westwood A (1987) 3-Hydroxydicarboxylic aciduria: a distinctive type of intermittent dicarboxylic aciduria of possible diagnostic significance.J Inher Metab Dis 10 (Supplement 2): 266–269.
Smeland TE, Nada M, Cuebas D, Schulz H (1992) NADPH-dependent β-oxidation of unsaturated fatty acids with double bonds extending from odd-numbered carbon atoms.Proc Natl Acad Sci USA 89: 6673–6677.
Tserng K-Y, ** S-J (1991) NADPH-dependent reductive metabolism ofcis-5 unsaturated fatty acids. A revised pathway for the β-oxidation of oleic acid.J Biol Chem 266: 11614–11620.
Venizelos N, Ijlst L, Wanders RJA, Hagenfeldt L (1994) β-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduria.Pediatr Res 36: 111–114.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Hagenfeldt, L., Venizelos, N. & von Döbeln, U. Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 18, 245–248 (1995). https://doi.org/10.1007/BF00711779
Issue Date:
DOI: https://doi.org/10.1007/BF00711779