Journal of Inherited Metabolic Disease

, Volume 17, Issue 3, pp 287–290 | Cite as

The segregation of glutaryl-CoA dehydrogenase deficiency and Refsum syndrome in a family

  • E. Christensen
  • N. J. Brandt
  • T. Rosenberg
  • K. Bömers
  • C. Jakobs
Short Communication
  • 29 Downloads

Keywords

Public Health Internal Medicine Dehydrogenase Deficiency 

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References

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Copyright information

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

Authors and Affiliations

  • E. Christensen
    • 1
  • N. J. Brandt
    • 1
  • T. Rosenberg
    • 2
  • K. Bömers
    • 3
  • C. Jakobs
    • 4
  1. 1.Section of Clinical GeneticsUniversity Department of Paediatrics, RigshospitaletCopenhagenDenmark
  2. 2.National Eye Clinic for the Visually ImpairedHellerupDenmark
  3. 3.Neurological DepartmentEsbjerg CentralsygehusEsbjergDenmark
  4. 4.Department of PaediatricsFree University HospitalAmsterdamThe Netherlands

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