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Severe neonatal galactose-dependent disease with low-normal epimerase activity

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Holton JB (1990) Galactose disorders: an overview.J Inher Metab Dis 13: 476–486.

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  • Segal S (1989) Disorders of galactose metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 453–480.

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Authors and Affiliations

  1. Institut de Bioquímica Clínica, Spain

    M. D. Boleda, M. L. Girós, P. Briones & S. Balaguer

  2. CSIC, Barcelona, Spain

    P. Briones

  3. Hospital Dr Peset, Valencia, Spain

    A. Sanchís

  4. Hospital Sant Joan de Déu, Barcelona, Spain

    L. Alvarez

  5. Department of Child Health, Children's Hospital, Bristol, UK

    J. B. Holton

Authors
  1. M. D. Boleda
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  2. M. L. Girós
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  3. P. Briones
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  4. A. Sanchís
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  5. L. Alvarez
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  6. S. Balaguer
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  7. J. B. Holton
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Additional information

Correspondence: Institut de Bioquímica Clínica, Avinguda Flor de Maig s/n, Apartat de Correus 137, 08290 Cerdanyola, Barcelona, Spain

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Boleda, M.D., Girós, M.L., Briones, P. et al. Severe neonatal galactose-dependent disease with low-normal epimerase activity. J Inherit Metab Dis 18, 88–89 (1995). https://doi.org/10.1007/BF00711385

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  • DOI: https://doi.org/10.1007/BF00711385

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