Glutathionuria
| Glutathionuria | |
|---|---|
| Other names | Gamma-glutamyl transpeptidase deficiency[1] |
 | |
| Glutathione | |
Glutathionuria is the presence of
inborn error of metabolism.[2]
The condition has been identified in five patients.[3]
References
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Gamma glutamyl transpeptidase deficiency". www.orpha.net. Retrieved 14 April 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - PMID 238530.
- ISBN 978-3-540-28783-4. Retrieved 1 May 2011.
External links