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It was also the tipping point for the man who would ultimately help bring him down

(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

10.1016/j.autrev.2023.103358 160 WeberE.GoveroverY.DeLucaJ

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