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