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Name: glutathione synthetase deficiency genereview Trimethylaminuria, Dimethylglycine Dehydrogenase and Disorders in the Metabolism of ATP-binding Cassette Transporter Defects and
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ATP binding Cassette Transporter Defects and Their Roles in Hepatic Diseases Disorders of Peptide and Amine Metabolism Springer Nature Link GLUTATHIONE SYNTHESIS PMC Molybdenum Cofactor Deficiency in Humans A rare case of Glutathione Synthetase Deficiency in a newborn with normal neurological development on follow up ScienceDirect Multiple congenital anomalies in two fetuses with glutathionesynthetase deficit (GSS) Jury 2024 Clinical Genetics Wiley Online Library

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319 (Pt 1), 117190

The spectra of DNApyocyanin mixtures confirm that DNA binds to pyocyanin with statistically significant changes in peak intensity ( 0.05) of 30 to 40% and 60 to 80% reduction in its biofilm thickness and total biofilm biomass, respectively (Table 2)