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Description
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Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter
doi: 10.1053/j.jrn.2021.03.009
146 WuY.HurrenR.MacLeanN.GrondaM.JitkovaY.SukhaiM
