Biochemical and electrophoretic studies of -galactosidase in normal man, in patients with Fabry's disease, and in Equidae.

Podobne knjige/članki

• Fabry's disease: evidence for a physically altered -galactosidase.
  od: Ho, M W, et al.
  Izdano: (1972)
• Variability of -galactosidase A and B in different tissues of man.
  od: Beutler, E, et al.
  Izdano: (1973)
• Fabry's disease: absence of an -galactosidase isozyme.
  od: Wood, S, et al.
  Izdano: (1972)
• Mutant α-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular processing by 1-deoxygalactonojirimycin
  od: Ishii, Satoshi, et al.
  Izdano: (2007)
• Glucocerebrosidase processing in normal fibroblasts and in fibroblasts from patients with type I, type II, and type III Gaucher disease.
  od: Beutler, E, et al.
  Izdano: (1986)