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Acute neonatal citrullinaemia

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Coude, F. X., Ogier, H., Marsac, C., Munnich, A., Charpentier, C. and Saudubray, J. M. Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.Pediatrics 68 (1981) 914

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  • Okken, A., Van der Bly, J. F. and Hommes, F. A. Citrullinemia and brain damage.Pediatr. Res. 7 (1973) 52–53

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  • Walser, M. Urea cycle disorders and other hereditary hyperammonemic syndromes. In Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.)The Metabolic Basis of Inherited Disease. 5th Edn. McGraw-Hill, New York, 1983, pp. 402–438.

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Authors and Affiliations

  1. Department of Chemical Pathology, The Children's Hospital, Sheffield, UK

    M. J. Bennett

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

    P. R. F. Dear

  3. Department of Chemical Pathology, St. James' University Hospital, Leeds, UK

    J. M. McGinlay

  4. University Sub-Department of Medical Genetics, 117 Manchester Road, Sheffield, UK

    R. G. F. Gray

Authors
  1. M. J. Bennett
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  2. P. R. F. Dear
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  3. J. M. McGinlay
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  4. R. G. F. Gray
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Bennett, M.J., Dear, P.R.F., McGinlay, J.M. et al. Acute neonatal citrullinaemia. J Inherit Metab Dis 7, 85 (1984). https://doi.org/10.1007/BF01805812

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  • DOI: https://doi.org/10.1007/BF01805812

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