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Description
Defects in the OCTN2 gene cause primary carnitine deficiency, further emphasizing the strategic position of OCTN2 in maintaining carnitine homeostasis [165]
In: AIFA, editor
This form of carnitine is crucial for transporting long-chain fatty acids into the mitochondria, where they are oxidised to produce energy
BURN FAT FASTER
doi: 10.1007/s12035-012-8278-5
Only this will stop the TSI antibodies from attacking the TSH receptors, which in turn will prevent the excess production of thyroid hormone
