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Journal of Inherited Metabolic Disease

, Volume 23, Issue 7, pp 760–764 | Cite as

Hyperketonaemia in glycerol kinase deficiency

  • D. R. Sjarif
  • L. Dorland
  • W. Sperl
  • T. J. de Koning
  • F. A. Beemer
  • B. T. Poll-The
  • M. Duran
Article

Keywords

Public Health Glycerol Internal Medicine Glycerol Kinase Glycerol Kinase Deficiency 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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REFERENCES

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  9. Sjarif DR, Sinke RJ, Duran M, et al (1998) Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency. J Med Genet 35: 650–656.Google Scholar
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Copyright information

© Kluwer Academic Publishers 2000

Authors and Affiliations

  • D. R. Sjarif
    • 1
  • L. Dorland
    • 1
  • W. Sperl
    • 2
  • T. J. de Koning
    • 1
  • F. A. Beemer
    • 3
  • B. T. Poll-The
    • 1
  • M. Duran
    • 4
  1. 1.Department of Pediatrics/Metabolic DiseasesWilhelmina Children's HospitalThe Netherlands
  2. 2.St. Johanns-Spital-Landesklinik fur Kinder- und JugendheilkundeSalzburgAustria
  3. 3.Department of Medical GeneticsUniversity Medical CenterUtrechtThe Netherlands
  4. 4.Department of Pediatrics/Metabolic DiseasesWilhelmina Children's HospitalThe Netherlands

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