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Paul CF, Ho VC, McGeown C, Christophers E, Schmidtmann B, Guillaume JC,

Front Endocrinol (Lausanne) (2020) 11:113

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The partial rescue of the above-described symptomatology can be ascribed to the activity of other transporters such as ATB 0,+ (SLC6A14), MCT9, and probably, OCTN1 (SLC22A4) that accept carnitine with a much lower affinity if compared to OCTN2

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