Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system

J Biol Chem. 1980 Sep 25;255(18):8381-4.
No abstract available

Publication types

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

MeSH terms

  • Antiporters
  • Child
  • Child, Preschool
  • Female
  • Glucose-6-Phosphatase / metabolism*
  • Glycogen Storage Disease Type I / enzymology*
  • Humans
  • Kinetics
  • Male
  • Microsomes, Liver / enzymology*
  • Monosaccharide Transport Proteins
  • Phosphotransferases / deficiency*
  • Reference Values

Substances

  • Antiporters
  • Monosaccharide Transport Proteins
  • SLC37A4 protein, human
  • glucose 6-phosphate(transporter)
  • Phosphotransferases
  • Glucose-6-Phosphatase