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A patient with α-ketoadipic and α-aminoadipic aciduria

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Fischer, M. H. and Brown, R. R. Tryptophan and lysine metabolism in alpha-aminoadipic aciduria.Am. J. Med. Genet. 5 (1980) 35–42

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  • Wendel, U., Rüdiger, H. W., Przyrembel, H. and Bremer, H. J. Alpha-ketoadipic aciduria: degradation studies with fibroblasts.Clin. Chim. Acta 58 (1975) 257–269

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Authors and Affiliations

  1. University Children's Hospital ‘Het Wilhemina Kinderziekenhuis’, Nieuwe Gracht 137, Utrecht, The Netherlands

    M. Duran, F. A. Beemer & S. K. Wadman

  2. Clinical Genetics Center Utrecht, P.O. Box, 18009, Utrecht, The Netherlands

    F. A. Beemer

  3. Medizinische Einrichtungen der Universität Düsseldorf, Düsseldorf, FRG

    U. Wendel

  4. Diakonessenhuis, Dept. Pediatrics, Utrecht, The Netherlands

    B. Janssen

Authors
  1. M. Duran
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  2. F. A. Beemer
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  3. S. K. Wadman
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  4. U. Wendel
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  5. B. Janssen
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Duran, M., Beemer, F.A., Wadman, S.K. et al. A patient with α-ketoadipic and α-aminoadipic aciduria. J Inherit Metab Dis 7, 61 (1984). https://doi.org/10.1007/BF01805803

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  • DOI: https://doi.org/10.1007/BF01805803

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