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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

When the seeds sown on 1/2 MS were exposed to cold stress, transgenic seeds began to germinate at day 7 whereas WT seeds were delayed 1 day

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These findings could explain the calcarine and parietal cell loss and gliosis seen in the rodent

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