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Ajona, D
10.1111/cns.13069 CNS Neurosci
5-oxoprolinase deficiency due to OPLAH gene mutation on chromosome 8q24.3 is a benign biochemical disorder of the gamma-glutamyl cycle that is transmitted as an autosomal recessive trait (04
One of the primary functions of Glutathione is to assist in the detoxification process
It is continuously retained in the body, so its administration is limited to one or two subcutaneous injections
Essential, yet not naturally found in the human body
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