Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.

Lignende værker

• Immunological studies of beta galactosidase in normal human liver and in GM1 gangliosidosis.
  af: Meisler, M, et al.
  Udgivet: (1974)
• Characterization of Hex S, the major residual beta hexosaminidase activity in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).
  af: Ikonne, J U, et al.
  Udgivet: (1975)
• GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene abnormalities in seven patients.
  af: Tanaka, A, et al.
  Udgivet: (1990)
• Therapeutic Potential of Intracerebroventricular Replacement of Modified Human β-Hexosaminidase B for GM2 Gangliosidosis
  af: Matsuoka, Kazuhiko, et al.
  Udgivet: (2011)
• Low levels of beta hexosaminidase A in healthy individuals with apparent deficiency of this enzyme.
  af: Navon, R, et al.
  Udgivet: (1976)