Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype–Phenotype Correlation

Authors

  • Yi-Chen Chen,

    1. Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
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  • Yin-Hsiu Chien,

    1. Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
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  • Pin-Wen Chen,

    1. Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
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  • Nelson Leung-Sang Tang,

    1. Department of Chemical Pathology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong
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  • Pao-Chin Chiu,

    1. Department of Pediatrics, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan
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  • Wuh-Liang Hwu,

    1. Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
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  • Ni-Chung Lee

    Corresponding author
    • Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan
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  • Communicated by Johannes Zschocke

Correspondence to: Ni-Chung Lee, Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan. E-mail: ncleentu@ntu.edu.tw

No abstract is available for this article.

Ancillary