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Defects in the OCTN2 gene cause primary carnitine deficiency, further emphasizing the strategic position of OCTN2 in maintaining carnitine homeostasis [165]

Rather than relying solely on willpower, these therapies help regulate appetite and metabolic signaling at the biological level

Carrer, M

10.1177/0269215520921506 105 Moss-MorrisR.HarrisonA

Circulating choline has been directly correlated with lung function in cystic fibrosis patients (28), and results of a pilot study in 10 patients suggested that choline supplementation may have utility in improving clinical outcomes in cystic fibrosis patients (29)