glutathione synthetase deficiency genereview Inborn errors in the metabolism of | Orphanet Journal of Rare Diseases Loss-of-function variant of SLC27A3 causes

Loss of function variant of SLC27A3 causes mitochondrial dysfunction and a metabolic neurodevelopmental disorder via impaired fatty acid transport Journal of Human Genetics Frontiers Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation Deficient Glutathione in the Pathophysiology of Mycotoxin Related Illness Brasil A case of severe glutathione synthetase deficiency with novel GSS mutations A case of severe glutathione synthetase deficiency with novel GSS mutations

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