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Many patients report reduced discomfort or improved function within 1-2 weeks

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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

It helps support both the adaptive and the innate immune systems by supporting T-cell production and influencing NK (Natural Killer) cells