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Description
international journal of clinical chemistry 2021
10.1016/s0165-6147(00)01575-3 51 ObeidR.AwwadH
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
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Vital source of energy during fasting, an easily absorbed micronutrient
