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[21] [22] Clinical significance [edit] Patients with mutations in the GSS gene develop glutathione synthetase (GSS) deficiency, an autosomal recessive disorder

Current dual agonists under investigation also include efinopegdutide and cotadutide

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The combination accelerates post-procedure healing, amplifies collagen induction, and produces visible improvements in skin texture, firmness, and radiance that neither treatment achieves as effectively on its own