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A significant group by time interaction was detected for plasma CRP ( p 0.05) for repetition count in the dominant leg (D-Leg), non-dominant leg (ND-Leg), or total count during the muscle damage exercise protocol endured on Week 5, indicating that volume was controlled

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Abstract Background: Systemic primary carnitine deficiency is an autosomal recessive disorder of the carnitine cycle caused by mutations in the SLC22A5 gene that encodes the carnitine transporter, organic cation transporter

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