Familial hyperlysinemias--multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase

Trans Am Clin Climatol Assoc. 1986:97:69-81.
No abstract available

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / enzymology*
  • Biological Evolution
  • Cells, Cultured
  • Fibroblasts / metabolism
  • Humans
  • Lysine / metabolism*
  • Multienzyme Complexes / deficiency*
  • Multienzyme Complexes / metabolism
  • Oxidoreductases Acting on CH-NH Group Donors / deficiency*
  • Saccharopine Dehydrogenases / deficiency*
  • Saccharopine Dehydrogenases / metabolism
  • Skin / metabolism

Substances

  • Multienzyme Complexes
  • Oxidoreductases Acting on CH-NH Group Donors
  • AASS protein, human
  • Saccharopine Dehydrogenases
  • saccharopine dehydrogenase (NADP+, lysine-forming)
  • Lysine