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Lu et al., 2018)

5-oxoprolinase deficiency due to OPLAH gene mutation on chromosome 8q24.3 is a benign biochemical disorder of the gamma-glutamyl cycle that is transmitted as an autosomal recessive trait (04

This lab-made peptide is thought to tell your muscles to behave like theyre exercising, even when youre not

The results showed that the hydrogel remained at the wound site for over 48 h, indicating favorable retention (Supplementary Fig

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