Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease

J Inherit Metab Dis. 1994;17(5):636-7. doi: 10.1007/BF00711609.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Carboxy-Lyases / deficiency*
  • Hemoglobin C Disease / enzymology
  • Hemoglobin C Disease / genetics*
  • Heterozygote*
  • Humans
  • Infant
  • Male

Substances

  • Carboxy-Lyases
  • malonyl-CoA decarboxylase