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Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder

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Journal of Inherited Metabolic Disease

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References

  • Englung PT (1993) The structure and biosynthesis of glycosyl phosphatidylinositol protein anchors.Annu Rev Biochem 62: 121–138.

    Google Scholar 

  • Lazarow PB, Moser HW (1989) Disorders of peroxisome biogenesis. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 1479–1509.

    Google Scholar 

  • Spranger JW, Opitz JM, Bidder U (1971) Heterogeneity of chondrodysplasia punctata.Hum Genet 11: 190–212.

    Google Scholar 

  • Stevens VL, Raetz CRH (1990) Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.J Biol Chem 265: 15653–15658.

    Google Scholar 

  • Van den Bosch H, Schutgens RBH, Wanders RJA, Tager M (1992) Biochemistry of peroxisomes.Annu Rev Biochem 61: 157–197.

    Google Scholar 

  • Wanders RJA, Heymans HSA, Schutgens RBH, Barth PG, Van den Bosch H, Tager JM (1988)J Neurol Sci 88: 1–39.

    Google Scholar 

  • Wanders RJA, Schumacher H, Heikoop J, Schutgens RBH, Tager JM (1992) Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder.J Inher Metab Dis 15: 389–391.

    Google Scholar 

  • Wanders RJA, Schutgens RBH, Barth PG, Tager JM, Van den Bosch H (1993) Postnatal diagnosis of peroxisomal disorders: a biochemical approach.Biochimie 75: 269–279.

    Google Scholar 

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Authors and Affiliations

  1. Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, 1105 AZ, Meibergdreef 9, Amsterdam, The Netherlands

    R. J. A. Wanders, C. Dekker, V. A. P. Hovarth & R. B. H. Schutgens

  2. Department of Biochemistry, E.C. Slater Institute, University of Amsterdam, Plantage Muidergracht 12, 1018 TV, Amsterdam, The Netherlands

    J. M. Tager

  3. Department of Pediatrics, A.Z. Sint. Jan, Ruddershove 10, 8000, Brugge, Belgium

    P. van Laer & D. Lecoutere

Authors
  1. R. J. A. Wanders
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  2. C. Dekker
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  3. V. A. P. Hovarth
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  4. R. B. H. Schutgens
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  5. J. M. Tager
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  6. P. van Laer
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  7. D. Lecoutere
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Wanders, R.J.A., Dekker, C., Hovarth, V.A.P. et al. Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder. J Inherit Metab Dis 17, 315–318 (1994). https://doi.org/10.1007/BF00711817

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  • DOI: https://doi.org/10.1007/BF00711817

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