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Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency

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Journal of Inherited Metabolic Disease

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Authors and Affiliations

  1. Institute of Metabolic Disease, Dallas, Texas, USA

    K. Hyland & L. A. Arnold

  2. Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas, USA

    K. Hyland & S. P. Sparagana

  3. Department of Neurology, Columbia Presbyterian Medical Center, New York, USA

    T. G. Nygaard

  4. Department of Neurology, University Virginia Health Sciences Center, Charlottesville, Virginia, USA

    J. M. Trugman

  5. Division of Genetics, Children's Hospital and Harvard Medical School Boston, Massachusetts, USA

    K. J. Swoboda

  6. Texas Scottish Rite Hospital for Children, Dallas, Texas, USA

    S. P. Sparagana

Authors
  1. K. Hyland
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  2. T. G. Nygaard
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  3. J. M. Trugman
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  4. K. J. Swoboda
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  5. L. A. Arnold
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  6. S. P. Sparagana
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Hyland, K., Nygaard, T.G., Trugman, J.M. et al. Oral phenylalanine loading profiles in symptomatic and asymptomatic gene carriers with dopa-responsive dystonia due to dominantly inherited GTP cyclohydrolase deficiency. J Inherit Metab Dis 22, 213–215 (1999). https://doi.org/10.1023/A:1005532610051

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  • DOI: https://doi.org/10.1023/A:1005532610051

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