glutathione synthetase deficiency genereview Participation in the Prevention of Cardiovascular Diseases Diagnosis and treatment of tyrosinemia
Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations Genetics in Medicine Frontiers Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation Loss of function variant of SLC27A3 causes mitochondrial dysfunction and a metabolic neurodevelopmental disorder via impaired fatty acid transport Journal of Human Genetics Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease New England Journal of Medicine 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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