Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts.

Những quyển sách tương tự

• Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”
  Bằng: Hsia, Y. Edward, et al.
  Được phát hành: (1971)
• Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts.
  Bằng: Wolf, B, et al.
  Được phát hành: (1980)
• Assignment of the alpha and beta chains of human propionyl-CoA carboxylase to genetic complementation groups.
  Bằng: Lam Hon Wah, A M, et al.
  Được phát hành: (1983)
• Biochemical differences between mutant propionyl-CoA carboxylases from two complementation groups.
  Bằng: Wolf, B, et al.
  Được phát hành: (1978)
• Cloning of functional alpha propionyl CoA carboxylase and correction of enzyme deficiency in pccA fibroblasts.
  Bằng: Stankovics, J, et al.
  Được phát hành: (1993)