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Rapid-Acting

Mov Disord 28(8):11381141

8) Primary carnitine deficiency (OMIM 212140), also known as carnitine uptake defect, carnitine transporter deficiency or systemic carnitine deficiency, is an autosomal recessive disorder of the carnitine cycle that results in defective fatty acid oxidation

Liver Fibrosis, but No Other Histologic Features, Is Associated with Long-term Outcomes of Patients with Nonalcoholic Fatty Liver Disease

Gas exchange reflects metabolic rate and overall energy expenditure suggesting that ALC-treatment likely enhanced energy production in the null mutants [30], [60], [79]

Biology of Reproduction 13, 154157.CrossRefGoogle ScholarPubMed Kiefer, C, Donzele, JL, Oliveira, RFMD, Suguisawa, L, Suguisawa, JM and Marques, ACW 2012