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6,20 Infants with G6PD deficiency and a mutation of uridine diphosphoglucuronate glucuronosyltransferase-1 gene promoter (UDPGT-1) are particularly susceptible to hyperbilirubinemia secondary to decreased liver clearance of bilirubin

By integrating neurocognitive peptides and supplements like DHHB into personalized care plans, we can also utilize synthetic peptides to mimic endogenous peptides, targeting specific receptors for therapeutic purposes and advancing personalized treatment approaches

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