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Description
(PubMed) Fielding R, Riede L, Lugo JP, Bellamine A
& Dixon, G
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
Always consult a healthcare provider before starting new supplements for complex chronic conditions
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