glutathione synthetase deficiency genereview Participation in the Prevention of Cardiovascular Diseases Molybdenum Cofactor Deficiency in Humans
Molybdenum Cofactor Deficiency in Humans Brasil A case of severe glutathione synthetase deficiency with novel GSS mutations A case of severe glutathione synthetase deficiency with novel GSS mutations Trimethylaminuria, Dimethylglycine Dehydrogenase Deficiency and Disorders in the Metabolism of Glutathione Springer Nature Link Loss of function variant of SLC27A3 causes mitochondrial dysfunction and a metabolic neurodevelopmental disorder via impaired fatty acid transport Journal of Human Genetics Nineteen year follow up of a patient with severe glutathione synthetase deficiency Journal of Human Genetics
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