Biotin-response Organicaciduria: MULTIPLE CARBOXYLASE DEFECTS AND COMPLEMENTATION STUDIES WITH PROPIONICACIDEMIA IN CULTURED FIBROBLASTS

Lignende værker

• Evidence for a defect of holocarboxylase synthetase activity in cultured lymphoblasts from a patient with biotin-responsive multiple carboxylase deficiency.
  af: Saunders, M E, et al.
  Udgivet: (1982)
• Propionicacidemia: absence of alpha-chain mRNA in fibroblasts from patients of the pccA complementation group.
  af: Lamhonwah, A M, et al.
  Udgivet: (1987)
• Acetyl CoA carboxylase in cultured fibroblasts: differential biotin dependence in the two types of biotin-responsive multiple carboxylase deficiency.
  af: Packman, S, et al.
  Udgivet: (1984)
• Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.
  af: Burri, B J, et al.
  Udgivet: (1981)
• Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts.
  af: Gravel, R A, et al.
  Udgivet: (1977)