glutathione synthetase deficiency smear as a Cause of Hereditary Hemolytic Disease Frontiers | Case report: A

Frontiers Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation Frontiers Glucose 6 Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity Glutathione Synthetase Deficiency StoryMD A rare case of Glutathione Synthetase Deficiency in a newborn with normal neurological development on follow up ScienceDirect Inborn errors in the metabolism of glutathione Orphanet Journal of Rare Diseases Springer Nature Link Frontiers Usefulness of NGS for Diagnosis of Dominant Beta Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases

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