X‐linked adrenoleukodystrophy: Identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl‐CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts
- 1 June 1988
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 11 (S2), 173-177
- https://doi.org/10.1007/bf01804228
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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- Peroxisomal fatty acid β-oxidation in human skin fibroblasts: X-linked adrenoleukodystrophy, a peroxisomal very long chain fatty acyl-CoA synthetase deficiency?Journal of Inherited Metabolic Disease, 1987
- Studies on the peroxisomal oxidation of palmitate and lignocerate in rat liverBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1987
- Lignoceroyl‐CoASH ligase: enzyme defect in fatty acid β‐oxidation system in X‐linked childhood adrenoleukodystrophyFEBS Letters, 1986
- Metabolism of [17, 18-3H2]hexacosanoic acid and [15,16-3H2]lignoceric acid in cultured skin fibroblasts from patients with adrenoleukodystrophy (ALD) and adrenomyeloneuropathy (AMN)Journal of the Neurological Sciences, 1985
- Adrenoleukodystrophy: Survey of 303 cases: Biochemistry, diagnosis, and therapyAnnals of Neurology, 1984
- Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.Proceedings of the National Academy of Sciences, 1984
- AdrenoleukodystrophyNeurology, 1984
- Adrenoleukodystrophy: Impaired oxidation of long chain fatty acids in cultured skin fibroblasts and adrenal cortexBiochemical and Biophysical Research Communications, 1981