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Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder

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Journal of Inherited Metabolic Disease

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References

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Authors and Affiliations

  1. Dept of Pediatrics and Clinical Biochemistry, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands

    R. J. A. Wanders & R. B. H. Schutgens

  2. Dept of Biochemistry, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands

    J. Heikoop & J. M. Tager

  3. Krankenhaus Renscheid-Lennep, Hans Potyka Strasse 28, Remscheid, Germany

    H. Schumacher

Authors
  1. R. J. A. Wanders
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  2. H. Schumacher
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  3. J. Heikoop
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  4. R. B. H. Schutgens
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  5. J. M. Tager
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Wanders, R.J.A., Schumacher, H., Heikoop, J. et al. Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder. J Inherit Metab Dis 15, 389–391 (1992). https://doi.org/10.1007/BF02435984

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  • DOI: https://doi.org/10.1007/BF02435984

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