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March 2, 1999Proceedings of the National Academy of SciencesOpen Access

Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency

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Authors

YWYuhuan WangCentre National de la Recherche ScientifiqueJYJing YeGuangxi Center for Disease Prevention and Control
Vadivel Ganapathy
Vadivel GanapathyUniversity of Southern California

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Cite This Study

Wang et al. (1999) studied this question.

synapsesocial.com/papers/6a82c2499192075d3cd4b508https://doi.org/10.1073/pnas.96.5.2356
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome1973 · 515 citations
  2. 2Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake1991 · 213 citations