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Argininosuccinase deficiency in a premature infant

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Brusilow, S. and Horwich, A. Urea cycle enzymes. In Scriver, C., Beaudet, A., Sly, W. and Valle, D. (eds.)The Metabolic Basis of Inherited Disease, 6th edn. McGraw Hill, New York, 1989, pp. 629–663

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  • Hudak, M., Jones, M. and Brusilow, S. Differentiation of transient hyperammonemia of the newborn and urea cycle enzyme defects by clinical presentation.J. Pediatr. 107 (1985) 712–719

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Author notes

  1. W. Wenner

    Present address: Children's Hospital of Philadelphia, 34th & Civic Center Blvd, 19104, Philadelphia, PA, USA

Authors and Affiliations

  1. Department of Pediatrics, University of California, Davis School of Medicine, Sacramento, CA, USA

    W. Wenner

  2. Department of Pediatrics and John F. Kennedy Institute, Johns' Hopkins University, School of Medicine, Baltimore, MD, USA

    A. Hamosh

Authors
  1. W. Wenner
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  2. A. Hamosh
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Wenner, W., Hamosh, A. Argininosuccinase deficiency in a premature infant. J Inherit Metab Dis 15, 285–286 (1992). https://doi.org/10.1007/BF01799647

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  • DOI: https://doi.org/10.1007/BF01799647

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