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10.1093/nar/gkab951 Summary Keywords glutathione synthetase deficiency, 5-oxoprolinuria, glutathione synthetase gene variation, newborn, inherited metabolic disease, case report Citation Wu X, Jiao J, Xia Y, Yan X, Liu Z, Cao Y and Ma L (2023) Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation

To view a copy of this licence, visit About this article Cite this article Mahani, M., Fallahi Nezhad, F., Khakbaz, F

This structural modification significantly extends its half-life and enhances resistance to proteolytic degradation, thereby enabling prolonged biological activity in vivo

Always test on a small area before using over larger areas of the skin

Screening for MTHFR Mutations If you fall under any of the following categories, you may consider screening for potential MTHFR mutation

these side effects are inherent with intravenous infusion of any substance