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[3] In humans, defects in GSS are inherited in an autosomal recessive way and are the cause of severe metabolic acidosis, 5-oxoprolinuria, increased rate of haemolysis, and defective function of the central nervous system

Triple receptor agonism (GLP-1 + GIP + Glucagon) Phase 2 clinical trial data published Weekly administration in research protocols Emerging research compound with significant interest AOD-9604 AOD-9604 is a modified fragment of human growth hormone (amino acids 177-191)

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