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Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases PDF) A case of severe glutathione synthetase deficiency with novel GSS mutations Glutamate dehydrogenase hyperinsulinism: mechanisms, diagnosis, and treatment Orphanet Journal of Rare Diseases Springer Nature Link Glutathione synthetase deficiency MedLink Neurology Frontiers Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation
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