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Description
It is typically administered intravenously or intramuscularly
However, the capacity to identify the other genotypes/subtypes was not improved in LiPA 2.0, since only 5-UTR information was used
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(More information) L-Carnitine supplementation is indicated for the treatment of primary systemic carnitine deficiency, which is caused by mutations in the gene that codes for the carnitine transporter, OCTN2
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