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Hereditary xanthinuria and Ehlers-Danlos syndrome

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Holmes EW, Wyngaarden JB (1989) Hereditary xanthinuria. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 1085–1094.

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Authors and Affiliations

  1. Department of Medicine, University of Alicante, Polig. Caramanchel s./n., 03800, Alcoy, Spain

    B. Roca, C. Calabuig & M. Arenas

  2. Department of Biochemistry, Hospital ‘Virgen de los Lirios’, S.V.S., University of Alicante, Polig. Caramanchel s./n., 03800, Alcoy, Spain

    J. Sastre

Authors
  1. B. Roca
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  2. C. Calabuig
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  3. J. Sastre
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  4. M. Arenas
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Roca, B., Calabuig, C., Sastre, J. et al. Hereditary xanthinuria and Ehlers-Danlos syndrome. J Inherit Metab Dis 15, 881–882 (1992). https://doi.org/10.1007/BF01800226

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  • DOI: https://doi.org/10.1007/BF01800226

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