Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area

Background: Primary carnitine deficiency (PCD) is attributed to a variation in the SLC22A5 (OCTN2) gene which encodes the key protein of the carnitine cycle, the OCTN2 carnitine transporter. PCD is typically identified in childhood by either hypoketotic hypoglycemia, or skeletal and cardiac myopathy...

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Main Authors: Wei Zhou (Author), Huizhong Li (Author), Ting Huang (Author), Yan Zhang (Author), Chuanxia Wang (Author), Maosheng Gu (Author)
Format: Book
Published: Frontiers Media S.A., 2019-02-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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