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ATP binding Cassette Transporter Defects and Their Roles in Hepatic Diseases Loss of function variant of SLC27A3 causes mitochondrial dysfunction and a metabolic neurodevelopmental disorder via impaired fatty acid transport Journal of Human Genetics Pyruvate Dehydrogenase Complex Deficiency: A Review of Treatments and Case Series Multiple congenital anomalies in two fetuses with glutathionesynthetase deficit (GSS) Jury 2024 Clinical Genetics Wiley Online Library A rare case of Glutathione Synthetase Deficiency in a newborn with normal neurological development on follow up ScienceDirect Overview of de novo glutathione synthesis . Reduced glutathione or GSH Download Scientific Diagram

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