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Biallelic truncating mutations in ZnT5/ZnT6 similarly lead to congenital disorders of glycosylation type II, presenting clinically with hypoglycosylated transferrin, osteopenia, developmental delay and multisystem involvement 78

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CRE-treated animals indicated a significantly higher activity of GPx than exposed nonCRE- or CRE-AgNPtreated animals

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Storage Instructions Handling and Storage Tips: Keep peptides cold and away from light once received