Biochemical differences between mutant propionyl-CoA carboxylases from two complementation groups.

Ítems similars

• Heterozygote Expression in Propionyl Coenzyme A Carboxylase Deficiency: DIFFERENCES BETWEEN MAJOR COMPLEMENTATION GROUPS
  per: Wolf, Barry, et al.
  Publicat: (1978)
• Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts.
  per: Wolf, B, et al.
  Publicat: (1980)
• Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”
  per: Hsia, Y. Edward, et al.
  Publicat: (1971)
• Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts.
  per: Gravel, R A, et al.
  Publicat: (1977)
• Assignment of the alpha and beta chains of human propionyl-CoA carboxylase to genetic complementation groups.
  per: Lam Hon Wah, A M, et al.
  Publicat: (1983)