Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease

J Inherit Metab Dis. 1993;16(2):288-91. doi: 10.1007/BF00710267.
No abstract available

Publication types

  • Review

MeSH terms

  • Gaucher Disease / enzymology
  • Gaucher Disease / genetics*
  • Gaucher Disease / physiopathology
  • Glucosylceramidase / deficiency
  • Glucosylceramidase / genetics
  • Humans
  • Lysosomal Storage Diseases / enzymology
  • Lysosomal Storage Diseases / genetics*
  • Lysosomal Storage Diseases / physiopathology
  • Lysosomes / metabolism

Substances

  • Glucosylceramidase