Frontiers Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease New England Journal of Medicine Glutathione Synthetase (13G3) Rabbit Monoclonal Antibody Glutathione: pharmacological aspects and implications for clinical use Geriatric Care
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glutathione synthetase deficiency symptoms Mitochondrial Glutathione in Cellular Redox Homeostasis and Disease Manifestation