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

J Inherit Metab Dis. 1988;11 Suppl 2:173-7. doi: 10.1007/BF01804228.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenoleukodystrophy / enzymology
  • Adrenoleukodystrophy / genetics*
  • Cell Fractionation / methods
  • Cells, Cultured
  • Coenzyme A Ligases / deficiency*
  • Diffuse Cerebral Sclerosis of Schilder / genetics*
  • Fibroblasts
  • Genetic Linkage
  • Humans
  • Microbodies / analysis
  • Microbodies / enzymology*
  • Skin
  • X Chromosome

Substances

  • Coenzyme A Ligases