Adrenoleukodystrophy and other peroxisomal diseases

This publication has 23 references indexed in Scilit:

• Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy
  Human Molecular Genetics, 1993
• Selective and ATP-Dependent Translocation of Peptides by the MHC-Encoded Transporter
  Science, 1993
• ABC Transporters: From Microorganisms to Man
  Annual Review of Cell Biology, 1992
• BIOCHEMISTRY OF PEROXISOMES
  Annual Review of Biochemistry, 1992
• Nucleotide sequence of the human 70 kDa peroxisomal membrane protein: a member of ATP-binding cassette transporters
  Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1992
• Linkage analysis in X-linked adrenoleukodystrophy and application in post-and prenatal diagnosis
  Human Genetics, 1991
• A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genes
  Genomics, 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 fibroblasts
  Journal of Inherited Metabolic Disease, 1988
• Linkage of adrenoleukodystrophy to a polymorphic DNA probe
  Annals of Neurology, 1987
• First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe
  Human Genetics, 1985