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At one year follow-up, both groups achieved significant and sustained improvement in weight loss, with no differences between the groups
This natural presence indicates that the molecule plays a role in the healthy development of the nursing infant
Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)
Its anti-inflammatory actions may help alleviate systemic inflammation and, indirectly, enhance upper airway neuromuscular stability, thus reducing airway collapsibility (48)
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