Fetal hexosaminidase A in mother's serum: pitfalls for carrier detection and prospects for prenatal diagnoses of GM2 gangliosidoses.

Lignende værker

• Frequency of hexosaminidase A variant alleles among Ashkenazi Jews and prenatal diagnosis of GM2 gangliosidosis.
  af: Navon, R, et al.
  Udgivet: (1985)
• Combined replacement effects of human modified β-hexosaminidase B and GM2 activator protein on GM2 gangliosidoses fibroblasts
  af: Kitakaze, Keisuke, et al.
  Udgivet: (2016)
• The GM1 and GM2 Gangliosidoses: Natural History and Progress toward Therapy
  af: Regier, Debra S., et al.
  Udgivet: (2016)
• Possible role of autoantibodies in the pathophysiology of GM2 gangliosidoses
  af: Yamaguchi, Akira, et al.
  Udgivet: (2004)
• Thymic Alterations in GM2 Gangliosidoses Model Mice
  af: Kanzaki, Seiichi, et al.
  Udgivet: (2010)