Disease: Glutathionuria
- Characterization and physiological function of rat renal gamma-glutamyltranspeptidase
- Glutathionuria: gamma-glutamyl transpeptidase deficiency
- Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase
- Inborn errors in the metabolism of glutathione
- Inhibition of gamma-glutamyl transpeptidase and induction of glutathionuria by gamma-glutamyl amino acids
- L-2-oxothiazolidine-4-carboxylate supplementation in murine gamma-GT deficiency
- Mice with genetic gamma-glutamyl transpeptidase deficiency exhibit glutathionuria, severe growth failure, reduced life spans, and infertility
- New aspects of glutathione metabolism and translocation in mammals
- Translocation of intracellular glutathione to membrane-bound gamma-glutamyl transpeptidase as a discrete step in the gamma-glutamyl cycle: glutathionuria after inhibition of transpeptidase
- Two Japanese brothers with hereditary gamma-glutamyl transpeptidase deficiency
- γ-glutamyl transpeptidase deficiency caused by a large homozygous intragenic deletion in GGT1