Response to Chen et al.: Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype–Phenotype Correlation

Authors

  • Marzia Pasquali,

    1. Division of Medical Genetics, /Pediatrics, University of Utah, Salt Lake City, Utah
    2. ARUP Institute for Clinical and Experimental Pathology®, ARUP Laboratories, Salt Lake City, Utah
    3. Department of Pathology, University of Utah, Salt Lake City, Utah
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  • Nicola Longo

    Corresponding author
    1. ARUP Institute for Clinical and Experimental Pathology®, ARUP Laboratories, Salt Lake City, Utah
    2. Department of Pathology, University of Utah, Salt Lake City, Utah
    • Division of Medical Genetics, /Pediatrics, University of Utah, Salt Lake City, Utah
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  • Communicated by Johannes Zschocke

  • Contract grant sponsor: National Institutes of Health (R01 DK 53824).

Correspondence to: Nicola Longo, Division of Medical Genetics, Department of Pediatrics, University of Utah, 2C412 SOM, 50 North Mario Capecchi Drive, Salt Lake City, Utah 84132. E-mail: Nicola.Longo@hsc.utah.edu

No abstract is available for this article.

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