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Pyrimidine metabolism in hereditary orotic aciduria

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Morishita H, Kokubo M, Sumi S, et al (1986) The first case of hereditary orotic aciduria in Japan. Nipponshonikagakugakkaizasshi 90: 2775–2778. (In Japanese with English abstract)

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  • Ohba S, Kidouchi K, Katoh T, et al (1991) Automated determination of orotic acid, uracil and pseudouridine in urine by high-performance liquid chromatography with column switching. J Chromatogr 568: 325–332.

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  • Webster DR, Becroft DMO, Suttle DP (1995) Hereditary orotic aciduria and other disorders of pyrimidine metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 7th edn. New York: McGraw-Hill, 1799–1837.

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Authors and Affiliations

  1. Department of Pediatrics, Nagoya City Child Welfare Center, Nagoya, Japan

    S. Sumi

  2. Department of Pediatrics, Nagoya City University Medical School, Nagoya, Japan

    S. Sumi, M. Suchi, H. Morishita, S. Ohba & Y. Wada

  3. Department of Pediatrics, Nagoya City Higashi General Hospital, Nagoya, Japan

    K. Kidouchi

Authors
  1. S. Sumi
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  2. M. Suchi
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  3. K. Kidouchi
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  4. H. Morishita
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  5. S. Ohba
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  6. Y. Wada
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Sumi, S., Suchi, M., Kidouchi, K. et al. Pyrimidine metabolism in hereditary orotic aciduria. J Inherit Metab Dis 20, 104–105 (1997). https://doi.org/10.1023/A:1005330127995

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  • DOI: https://doi.org/10.1023/A:1005330127995

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