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The liver metabolises Dihexa via both Phase I oxidation (primarily CYP3A4) and Phase II conjugation (glucuronidation), converting the active compound into inactive metabolites that are renally excreted
The correct sequence of the GOI was confirmed by the Sanger sequencing service of Microsynth
9 Details on the distribution of G6PD deficiency among various population groups is presented elsewhere
The human body naturally produces L-arginine
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