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highlight a potential pharmacogenomic approach to supplementation, Assel and colleagues found no strong evidence for genotype-based treatment strategies

(Etiology) Carnitine-Acylcarnitine Translocase Deficiency Disorder is caused by mutations in the SLC25A20 gene, which provides instructions for making an enzyme called carnitine-acylcarnitine translocase (CACT), which is essential for fatty acid oxidation (a multistep process that breaks down (metabolizes) fats and converts them into energy) Fatty acid oxidation takes place within mitochondria

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We recommend that you seek advice from a fully qualified healthcare professional before consuming any of these products especially if you are taking other medications or pregnant

[DOI] [PMC free article] [PubMed] [Google Scholar] 24.Muoio D.M

Maca ( Lepidium meyenii ) Maca root is consumed either fresh or dried and has a distinctive taste and aroma