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Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)
bioRxiv 2023:2023.2008
For example, Piagnerelli et al
Competing interests AM and SS are co-founders of Bash Biotech Inc, USA and XL is employed by Bash Biotech Inc, USA
The dehydrogenation reaction catalyzed by glucose 6-phosphate dehydrogenase is the committed step in this pathway
The neurocircuitry of fear, stress, and anxiety disorders
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