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Transient 5-oxoprolinuria in a very low-birthweight infant

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Larsson, A., Mattsson, B., Wauters, E. A. K., Van Gool, J. D., Duran, M. and Wadman, S.K. 5-Oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers — a new inborn error of γ-glutamyl cycle.Acta Paediatr. Scand. 70 (1981) 301–308

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  • Wellner, V. P., Sekura, R., Meister, A. and Larsson, A. Glutathione synthetase deficiency, an inborn error of metabolism involving the γ-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).Proc. Natl. Acad. Sci. USA 71 (1974) 2505–2509

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Authors and Affiliations

  1. Department of Pediatrics, Akita University School of Medicine, 1-1-1, Hondo, 010, Akita, Japan

    A. Goto, A. Ishida, R. Goto, K. Hayasaka, K. Nanao, A. Yamashita & G. Takada

  2. Department of Pediatrics, Gifu University School of Medicine, 40, Tsukasamachi, 500, Gifu, Japan

    S. Yamaguchi

Authors
  1. A. Goto
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  2. A. Ishida
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  3. R. Goto
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  4. K. Hayasaka
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  5. K. Nanao
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  6. A. Yamashita
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  7. S. Yamaguchi
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  8. G. Takada
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Goto, A., Ishida, A., Goto, R. et al. Transient 5-oxoprolinuria in a very low-birthweight infant. J Inherit Metab Dis 15, 284–285 (1992). https://doi.org/10.1007/BF01799646

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  • DOI: https://doi.org/10.1007/BF01799646

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