glutathione s transferase deficiency

glutathione s transferase deficiency Frontiers Frontiers | Regulation of epigenetic

Name: glutathione s transferase deficiency Frontiers Frontiers | Regulation of epigenetic
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Description

These primary data suggest that carriers of the Thr92Ala polymorphism may experience inadequate intracerebral T3 availability despite standard replacement therapy, contributing to persistent symptoms

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Wang F, Dou P, Wei W, Liu PJ

Ethics approval and consent to participate This review synthesizes previously published scientific studies and does not include any experiments involving human subjects, animals, or the acquisition of new clinical information