Cystathionase deficiency: evidence for genetic heterogeneity in primary cystathioninuria

Pediatr Res. 1978 Feb;12(2):125-33. doi: 10.1203/00006450-197802000-00012.
No abstract available

Publication types

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

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / enzymology
  • Amino Acid Metabolism, Inborn Errors / genetics*
  • Animals
  • Binding Sites, Antibody
  • Binding, Competitive
  • Cell Line
  • Cystathionine / urine*
  • Cystathionine gamma-Lyase / genetics
  • Cystathionine gamma-Lyase / immunology*
  • Cystathionine gamma-Lyase / metabolism
  • Fetus / enzymology
  • Haplorhini
  • Humans
  • Immune Sera / pharmacology
  • Immunodiffusion
  • Immunoelectrophoresis
  • In Vitro Techniques
  • Lyases / immunology*
  • Pyridoxal Phosphate / pharmacology
  • Rats

Substances

  • Immune Sera
  • Cystathionine
  • Pyridoxal Phosphate
  • Lyases
  • Cystathionine gamma-Lyase