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Lethal ornithine transcarbamylase deficiency in a female neonate

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Batshaw, M. L., Thomas, G. H. and Brusilow, S. W. New approaches to the diagnosis and treatment of inborn errors of urea synthesis.Pediatrics 68 (1981) 290–297

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  • Gray, R. G. F., Black, J. A., Lyons, V. H. and Pollitt, R. J. Ornithine transcarbamylase deficiency: Enzyme studies on a further case and a method of diagnosis using plasma enzyme ratios.Pediatr. Res. 10 (1976) 918–923

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Authors and Affiliations

  1. Baystate Medical Center, Springfield, MA, USA

    N. Girgis, V. McGravey & B. L. Shah

  2. Massachusetts General Hospital, Boston, MA, USA

    J. Herrin & V. E. Shih

Authors
  1. N. Girgis
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  2. V. McGravey
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  3. B. L. Shah
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  4. J. Herrin
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  5. V. E. Shih
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Girgis, N., McGravey, V., Shah, B.L. et al. Lethal ornithine transcarbamylase deficiency in a female neonate. J Inherit Metab Dis 10, 274–275 (1987). https://doi.org/10.1007/BF01800079

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  • DOI: https://doi.org/10.1007/BF01800079

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