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Hepatic metabolites and uric acid excretion in fructose-1,6-diphosphatase deficiency

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Journal of Inherited Metabolic Disease

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References

  • DeVivo, D. C., Haymond, M. W., Leckie, M. P., Bussman, Y. L., McDougal, D. B. Jr. and Pagliara, A. S. The clinical and biochemical implications of pyruvate carboxylase deficiency.J. Clin. Endocrinol. Metab. 45 (1977) 1281–1296

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  • Pagliara, A. S., Karl, I. E., Keating, J. P., Brown, B. I. and Kipnis, D. M. Hepatic fructose-1,6-diphosphatase deficiency.J. Clin. Invest. 51 (1972) 2115–2123

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Authors and Affiliations

  1. Unidad de Genética de la Nutrición, Instituto de Investigaciones Biomedicas, Apdo. Postal 101–48, 04530, México DF, México

    A. Velázquez

  2. Hospital Nacional de Niños, Caja Costarricense de Seguro Social, San José, Costa Rica

    C. DeCéspedes

  3. Pediatric Neurology Division, College of Physicians and Surgeons of Colombia University, New York, NY, USA

    D. C. DeVivo

  4. Department of Pediatrics, Childrens Hospital of Los Angeles, Los Angeles, CA, USA

    G. Costin

  5. Medical Genetics Division, Childrens Hospital of Los Angeles, Los Angeles, CA, USA

    K. N. F. Shaw

Authors
  1. A. Velázquez
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  2. C. DeCéspedes
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  3. D. C. DeVivo
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  4. G. Costin
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  5. K. N. F. Shaw
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Velázquez, A., DeCéspedes, C., DeVivo, D.C. et al. Hepatic metabolites and uric acid excretion in fructose-1,6-diphosphatase deficiency. J Inherit Metab Dis 11, 303–304 (1988). https://doi.org/10.1007/BF01800375

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  • DOI: https://doi.org/10.1007/BF01800375

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