Adrenoleukodystrophy gene: Unexpected homology to a protein involved in peroxisome biogenesis
- 31 December 1993
- Vol. 75 (3-4) , 293-302
- https://doi.org/10.1016/0300-9084(93)90089-b
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Brain MRI and electrophysiologic abnormalities in preclinical and clinical adrenomyeloneuropathyNeurology, 1992
- Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liverBiochemical Journal, 1991
- Adrenoleukodystrophy presenting as addison's disease in children and adultsTrends in Endocrinology & Metabolism, 1991
- Topographical localization of peroxisomal acyl-CoA ligases: differential localization of palmitoyl-CoA and lignoceroyl-CoA ligasesBiochemistry, 1990
- 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 fibroblastsJournal of Inherited Metabolic Disease, 1988
- Linkage of adrenoleukodystrophy to a polymorphic DNA probeAnnals of Neurology, 1987
- Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red PigmentsScience, 1986
- Lignoceroyl‐CoASH ligase: enzyme defect in fatty acid β‐oxidation system in X‐linked childhood adrenoleukodystrophyFEBS Letters, 1986
- First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probeHuman Genetics, 1985
- INDIVIDUAL PEROXISOMAL βT‐OXIDATION ENZYMES*Annals of the New York Academy of Sciences, 1982