glutathione synthetase deficiency genereview SYNTHESIS 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 Inborn errors of enzymes in glutamate metabolism PMC Brasil A case of severe glutathione synthetase deficiency with novel GSS mutations A case of severe glutathione synthetase deficiency with novel GSS mutations Disorders of Peptide and Amine Metabolism Springer Nature Link Frontiers Leigh Syndrome: A Tale of Two Genomes

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