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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
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Moreover, glutathione is synthesized in the transsulfuration pathway, where sulfur availability is crucial
We chose the carbon tape as the substrate in this case and drop-casted the sample onto it
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