Sandbox Reserved 771: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 57: | Line 57: | ||
Though reduced levels of GSH have been observed in patients with Alzheimers and Parkinsons, inborn errors in the endogenous GSS enzyme resulting in significantly low levels of GSH is believed to be the cause of a metabolic deficiency termed 5-oxoprolinuria. | Though reduced levels of GSH have been observed in patients with Alzheimers and Parkinsons, inborn errors in the endogenous GSS enzyme resulting in significantly low levels of GSH is believed to be the cause of a metabolic deficiency termed 5-oxoprolinuria. | ||
</StructureSection> | |||
==References== | ==References== | ||
<references/> | |||
1. http://www.ncbi.nlm.nih.gov/protein/NP_000169.1 | 1. http://www.ncbi.nlm.nih.gov/protein/NP_000169.1 | ||
