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5-Oxoprolinuria associated with 5-oxoprolinase deficiency; further evidence that this is a benign disorder

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Larsson A, Mattsson B, Wauters EAK et al (1981) 5-Oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers — A new inborn error of the gamma-glutamyl cycle.Acta Paediatr Scand 70: 301–307.

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  • Roesel RA, Hommes FA, Samper L (1981) Pyroglutamic aciduria (5-oxoprolinuria) without glutathione synthetase deficiency and with decreased pyroglutamate hydrolase activity.J Inher Metab Dis 4: 89–92.

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Authors and Affiliations

  1. Department of Chemical Pathology, St. James' University Hospital, LS9 7TF, Leeds, UK

    M. J. Henderson

  2. Department of Paediatrics, St. James' University Hospital, LS9 7TF, Leeds, UK

    P. R. F. Dear

  3. Department of Paediatrics, University Hospital, Uppsala, Sweden

    A. Larsson & B. Carlsson

Authors
  1. M. J. Henderson
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  2. A. Larsson
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  3. B. Carlsson
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  4. P. R. F. Dear
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Henderson, M.J., Larsson, A., Carlsson, B. et al. 5-Oxoprolinuria associated with 5-oxoprolinase deficiency; further evidence that this is a benign disorder. J Inherit Metab Dis 16, 1051–1052 (1993). https://doi.org/10.1007/BF00711529

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  • DOI: https://doi.org/10.1007/BF00711529

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