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Hoboken, NJ, USA: 1988

Rare mutations in the SLC22A5 gene can cause a genetic condition called primary carnitine deficiency, which is usually discovered in infancy because it affects brain function, muscle function, and blood glucose levels

In autophagy-deficient cells, intracellular iron and lipid peroxidation were decreased, resulting in cells that could become resistant to erastin-induced ferroptosis [70]

Consult a physician prior to using this, or any dietary supplement