The molecular defect of ferrochelatase in a patient with erythropoietic protoporphyria.

Lignende værker

• Systematic analysis of molecular defects in the ferrochelatase gene from patients with erythropoietic protoporphyria.
  af: Rüfenacht, U B, et al.
  Udgivet: (1998)
• Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation.
  af: Bloomer, J, et al.
  Udgivet: (1998)
• Studies in porphyria: functional evidence for a partial deficiency of ferrochelatase activity in mitogen-stimulated lymphocytes from patients with erythropoietic protoporphyria.
  af: Sassa, S, et al.
  Udgivet: (1982)
• Cloning and expression of the defective genes from a patient with delta-aminolevulinate dehydratase porphyria.
  af: Ishida, N, et al.
  Udgivet: (1992)
• Modulation of the phenotype in dominant erythropoietic protoporphyria by a low expression of the normal ferrochelatase allele.
  af: Gouya, L., et al.
  Udgivet: (1996)