Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder
R. J. A. Wanders
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorC. Dekker
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorV. A. P. Hovarth
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorR. B. H. Schutgens
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorJ. M. Tager
Department of Biochemistry, E.C. Slater Institute, University of Amsterdam, Plantage Muidergracht 12, Amsterdam, 1018 TV The Netherlands
Search for more papers by this authorP. van Laer
Department of Pediatrics, A.Z. Sint. Jan, Ruddershove 10, Brugge, 8000 Belgium
Search for more papers by this authorD. Lecoutere
Department of Pediatrics, A.Z. Sint. Jan, Ruddershove 10, Brugge, 8000 Belgium
Search for more papers by this authorR. J. A. Wanders
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorC. Dekker
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorV. A. P. Hovarth
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorR. B. H. Schutgens
Department of Pediatric Clinical Biochemistry, University Hospital Amsterdam, Meibergdreef 9Amsterdam, 1105 AZ The Netherlands
Search for more papers by this authorJ. M. Tager
Department of Biochemistry, E.C. Slater Institute, University of Amsterdam, Plantage Muidergracht 12, Amsterdam, 1018 TV The Netherlands
Search for more papers by this authorP. van Laer
Department of Pediatrics, A.Z. Sint. Jan, Ruddershove 10, Brugge, 8000 Belgium
Search for more papers by this authorD. Lecoutere
Department of Pediatrics, A.Z. Sint. Jan, Ruddershove 10, Brugge, 8000 Belgium
Search for more papers by this author
References
- 1Englung PT (1993) The structure and biosynthesis of glycosyl phosphatidylinositol protein anchors. Annu Rev Biochem, 62: 121–138.
10.1146/annurev.bi.62.070193.001005 Google Scholar
- 2Lazarow PB, Moser HW, Scriver CR, Beaudet AL, Sly WS, Valle D (1989) Disorders of peroxisome biogenesis. In: The Metabolic Basis of Inherited Disease, 6th edn.. New York: McGraw-Hill, 1479–1509.
- 3Spranger JW, Opitz JM, Bidder U (1971) Heterogeneity of chondrodysplasia punctata. Hum Genet, 11: 190–212.
- 4Stevens VL, Raetz CRH (1990) Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis. J Biol Chem, 265: 15653–15658.
- 5Van den Bosch H, Schutgens RBH, Wanders RJA, Tager M (1992) Biochemistry of peroxisomes. Annu Rev Biochem, 61: 157–197.
- 6Wanders RJA, Heymans HSA, Schutgens RBH, Barth PG, Van den Bosch H, Tager JM (1988) J Neurol Sci, 88: 1–39.
- 7Wanders 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.
- 8Wanders RJA, Schutgens RBH, Barth PG, Tager JM, Van den Bosch H (1993) Postnatal diagnosis of peroxisomal disorders: a biochemical approach. Biochimie, 75: 269–279.
