[Hereditary tyrosinemia type I].

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
Read More Add to Saved list
  • Author(s): Endo F;Endo F
  • Source:
    Ryoikibetsu shokogun shirizu [Ryoikibetsu Shokogun Shirizu] 1998 (18 Pt 1), pp. 130-3.
  • Publication Type:
    Journal Article; Review
  • Language:
    Japanese
  • Additional Information
    • Source:
      Publisher: Nihon Rinshōsha Country of Publication: Japan NLM ID: 9501926 Publication Model: Print Cited Medium: Print NLM ISO Abbreviation: Ryoikibetsu Shokogun Shirizu Subsets: MEDLINE
    • Publication Information:
      Original Publication: Ōsaka-shi : Nihon Rinshōsha, Heisei 5 [1993]-
    • Subject Terms:
      Amino Acid Metabolism, Inborn Errors*; Hydrolases/*deficiency ; Tyrosine/*blood; Genes, Recessive ; Humans ; Hydrolases/genetics ; Mutation
    • Number of References:
      17
    • Accession Number:
      42HK56048U (Tyrosine)
      EC 3.- (Hydrolases)
      EC 3.7.1.2 (fumarylacetoacetase)
    • Publication Date:
      Date Created: 19980520 Date Completed: 19980709 Latest Revision: 20131121
    • Publication Date:
      20240829
    • Accession Number:
      9590006