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Description
Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)
Polyphenols: A concise overview on the chemistry, occurrence, and human health
Figure 4 displays the lactate measures at rest as well as four and 14 minutes post-exercise
95% CI: 0.005 to 23 IU/L
