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Inborn errors of metabolism mainly include diseases such as fatty acid oxidation defects, mitochondrial dysfunctions, organic acidurias, as well as lysosomal and glycogen storage disorders

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[Journal of Inorganic Biochemistry, 2014, vol

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Stein, S

The findings demonstrated that the interactions between GLP-1/GLP-1R and HSA-DARPin/HSA persisted even after the amino acid substitution in GLP-1 and the formation of the fusion protein