glutathione synthetase deficiency genereview Participation in the Prevention of Cardiovascular 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 Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations Genetics in Medicine Nineteen year follow up of a patient with severe glutathione synthetase deficiency Journal of Human Genetics Trimethylaminuria, Dimethylglycine Dehydrogenase Deficiency and Disorders in the Metabolism of Glutathione Springer Nature Link A rare case of Glutathione Synthetase Deficiency in a newborn with normal neurological development on follow up ScienceDirect

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