Journal of Inherited Metabolic Disease

, Volume 17, Issue 3, pp 315–318

Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder

Authors

  • R. J. A. Wanders
    • Department of Pediatric Clinical BiochemistryUniversity Hospital Amsterdam
  • C. Dekker
    • Department of Pediatric Clinical BiochemistryUniversity Hospital Amsterdam
  • V. A. P. Hovarth
    • Department of Pediatric Clinical BiochemistryUniversity Hospital Amsterdam
  • R. B. H. Schutgens
    • Department of Pediatric Clinical BiochemistryUniversity Hospital Amsterdam
  • J. M. Tager
    • Department of Biochemistry, E.C. Slater InstituteUniversity of Amsterdam
  • P. van Laer
    • Department of PediatricsA.Z. Sint. Jan
  • D. Lecoutere
    • Department of PediatricsA.Z. Sint. Jan
Short Communication

DOI: 10.1007/BF00711817

Cite this article as:
Wanders, R.J.A., Dekker, C., Hovarth, V.A.P. et al. J Inherit Metab Dis (1994) 17: 315. doi:10.1007/BF00711817

Copyright information

© Society for the Study of Inborn Errors of Metabolism and Kluwer Academic Publishers 1994