glutathione synthetase deficiency smear

glutathione synthetase deficiency smear as a Cause of Hereditary Hemolytic Disease A rare case of Glutathione

Name: glutathione synthetase deficiency smear as a Cause of Hereditary Hemolytic Disease A rare case of Glutathione
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SKU: 79424444489
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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 Glucose 6 phosphate Dehydrogenase (G6PD) Deficiency A Laboratory Guide to Clinical Hematology Frontiers Usefulness of NGS for Diagnosis of Dominant Beta Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases

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Description

It prevents cell division by stabilizing -tubulin heterodimers in the microtubules, preventing depolymerization, and inhibiting the G2/M phase of the cell cycle, leading to cell death