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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

Intravenous glutathione is considered the most effective method, as it bypasses the digestive system and delivers glutathione directly into the bloodstream for optimal absorption - but there are safety risks involved

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Table 2: Variation of regional brain metabolite levels with diagnosis group, age, and sex as fixed effects in robust linear mixed-effects (LME) models