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Carnitine deficiency in autism: Mutations in enzymes involved in carnitine biosynthesis have been linked to autism spectrum disorders, indicating a broader systemic impact of carnitine beyond fertility
The latter acts as a chaperone for monocarboxylate transporter 1 (MCT1) and MCT4, facilitates their proper expression at the cell surface, and prevents their degradation
Overall, there is a strong association between common causes of ovarian reserve loss, such as aging, genetic variation, OS, radiation and chemotherapy, and ferroptosis, with disturbances in intracellular iron metabolism playing a central role in this process
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