Journal of Inherited Metabolic Disease

, Volume 20, Issue 3, pp 420–422

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of two new mutations

  • L. IJlst
  • W. Oostheim
  • J. P. N. Ruitter
  • R. J. A. Wanders
Article

DOI: 10.1023/A:1005310903004

Cite this article as:
IJlst, L., Oostheim, W., Ruitter, J.P.N. et al. J Inherit Metab Dis (1997) 20: 420. doi:10.1023/A:1005310903004

Copyright information

© Kluwer Academic Publishers 1997

Authors and Affiliations

  • L. IJlst
    • 1
  • W. Oostheim
    • 1
  • J. P. N. Ruitter
    • 1
  • R. J. A. Wanders
    • 1
    • 2
  1. 1.Department of Clinical ChemistryAcademical Medical Centre, University of AmsterdamAmsterdamThe Netherlands
  2. 2.Department of PaediatricsAmsterdamThe Netherlands

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