The leukodystrophies: a window to myelin

This publication has 15 references indexed in Scilit:

• Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease
  Nature Genetics, 1993
• Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.
  Proceedings of the National Academy of Sciences, 1991
• Major myelin proteolipid: The 4-α-helix topology
  The Journal of Membrane Biology, 1991
• Molecular Basis of Different Forms of Metachromatic Leukodystrophy
  New England Journal of Medicine, 1991
• A new mutation in the proteolipid protein (PLP) gene in a German family with pelizaeus‐merzbacher disease
  American Journal of Medical Genetics, 1991
• Molecular Genetics of X‐Linked Mutants
  Annals of the New York Academy of Sciences, 1990
• Structure of the arylsulfatase A gene
  European Journal of Biochemistry, 1990
• Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.
  Proceedings of the National Academy of Sciences, 1989
• Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.
  Proceedings of the National Academy of Sciences, 1989
• Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder.
  Proceedings of the National Academy of Sciences, 1989