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There are a bunch of other inborn errors of metabolism, including short-chain acyl-CoA dehydrogenase deficiency and medium-chain acyl-CoA dehydrogenase deficiency.[ref] Lets look at the inborn errors of metabolism involving carnitine: CPT2 gene: The CPT2 gene encodes the enzyme that moves fatty acids attached to carnitine into the inner membrane of the mitochondria
Comparing bioinformatic pipelines for microbial 16S rRNA amplicon sequencing
Medical science has known for decades about its target, the glucagon-like peptide-1 receptor (GLP-1R)
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