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B., Karall, D., de, Klerk H., Knerr, I., Koch, H
Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation
Fabbrocini A, et al
However, the actual increase in the proportion of fatty acid oxidation is limited by multiple factors
Absorption of D- and L-carnitine by the intestine and kidney tubule in the rat
D.EmeryS
