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Ornithine carbamoyltransferase deficiency presenting with chorea in a female

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Journal of Inherited Metabolic Disease

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REFERENCE

  • Brusilow S, Horwich AL (1995) Urea cycle enzymes. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1187–1232.

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Authors and Affiliations

  1. Department of Chemical Pathology, Women's and Children's Hospital, North Adelaide, Australia

    E. J. Wiltshire, N. K. Poplawski, M. G. Harbord & R. J. Harrison

  2. Department of Chemical Pathology, Women's and Children's Hospital, North Adelaide, Australia

    J. M. Fletcher

Authors
  1. E. J. Wiltshire
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  2. N. K. Poplawski
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  3. M. G. Harbord
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  4. R. J. Harrison
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  5. J. M. Fletcher
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Wiltshire, E.J., Poplawski, N.K., Harbord, M.G. et al. Ornithine carbamoyltransferase deficiency presenting with chorea in a female. J Inherit Metab Dis 23, 843–844 (2000). https://doi.org/10.1023/A:1026768904395

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  • DOI: https://doi.org/10.1023/A:1026768904395

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