A derangement in B 12 metabolism leading to homocystinemia, cystathioninemia and methylmalonic aciduria

Biochem Biophys Res Commun. 1969 Apr 10;35(1):121-6. doi: 10.1016/0006-291x(69)90491-4.
No abstract available

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / etiology*
  • Aminobutyrates / blood
  • Aminobutyrates / metabolism*
  • Brain / metabolism
  • Homocysteine / blood
  • Homocysteine / metabolism*
  • Homocysteine / urine
  • Homocystine / blood
  • Homocystine / metabolism
  • Homocystinuria / etiology
  • Humans
  • Infant
  • Kidney / enzymology
  • Kidney / metabolism
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Malonates / urine*
  • Metabolism, Inborn Errors / etiology*
  • Methionine / blood
  • Methionine / metabolism*
  • Methionine / urine
  • Sulfides / metabolism
  • Transferases / metabolism*
  • Vitamin B 12 / blood
  • Vitamin B 12 / metabolism*

Substances

  • Aminobutyrates
  • Malonates
  • Sulfides
  • Homocysteine
  • Homocystine
  • Methionine
  • Transferases
  • Vitamin B 12