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Dihydropyrimidinase deficiency presenting in infancy with severe developmental delay

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Journal of Inherited Metabolic Disease

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References

  • Brockstedt M, Jakobs C, Smit LME et al (1990) A new case of dihydropyrimidine dehydrogenase deficiency.J Inher Metab Dis 13: 121–124.

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  • Duran M, Rovers P, de Bree PK et al (1991) Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism.J Inher Metab Dis 14: 367–370.

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Authors and Affiliations

  1. Department of Chemical Pathology, St. James's Hospital, Leeds, UK

    M. J. Henderson

  2. Department of Paediatrics, Airedale General Hospital, Keighley, UK

    K. Ward

  3. Purine Research Laboratory, Guy's Hospital, London, UK

    H. A. Simmonds, J. A. Duley & P. M. Davies

Authors
  1. M. J. Henderson
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  2. K. Ward
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  3. H. A. Simmonds
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  4. J. A. Duley
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  5. P. M. Davies
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Henderson, M.J., Ward, K., Simmonds, H.A. et al. Dihydropyrimidinase deficiency presenting in infancy with severe developmental delay. J Inherit Metab Dis 16, 574–576 (1993). https://doi.org/10.1007/BF00711685

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  • DOI: https://doi.org/10.1007/BF00711685

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