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(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

Bohles H, Sewell AC, Wenzel D

Durante el proceso de la liplisis, los triglicridos se descomponen en dos fracciones

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Sex-specific genetic effects across biomarkers

Supplemented with carefully selected amino acids Our formula is also supplemented with L-Arginine, N-Acetyl-Cysteine and N-Acetyl-Carnitine