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279 ZhangM.HeY.SunX.LiQ.WangW.ZhaoA.et al (2014)
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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124 ZhangZ.YangX.LiuO.CaoX.TongJ.XieT.et al (2021)
After unsuccessful sleep induction with Mel, DexL was used in two cases as the second drug (both subjects fell asleep), and DexN was used in seven cases (6/7 subjects fell asleep)
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