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Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases pp 189–193Cite as

Disorders of Glycerol Metabolism

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References

  1. Beatty ME, Zhang YH, McCabe ERB, Steiner RD (2000) Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GIS. Molec Genet Metab 69:338–340

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Authors
  1. Katrina M. Dipple
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  2. Edward R.B. McCabe
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Editor information

Editors and Affiliations

  1. Division of Clinical Chemistry and Biochemistry, University Children’s Hospital, Steinwiesstrasse 75, 8032, Zurich, Switzerland

    Nenad Blau

  2. Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, 30, Guilford Street, London, WC1N 1EH, UK

    James Leonard

  3. Universitätsklinik für Kinder- und Jugendmedizin, Im Neuenheimer Feld 150, D-69120, Heidelberg, Germany

    Georg F. Hoffmann

  4. Division of Clinical & Metabolic Genetics, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada

    Joe T. R. Clarke

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© 2006 Springer-Verlag Berlin Heidelberg

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Dipple, K.M., McCabe, E.R. (2006). Disorders of Glycerol Metabolism. In: Blau, N., Leonard, J., Hoffmann, G.F., Clarke, J.T.R. (eds) Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-28962-3_19

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  • DOI: https://doi.org/10.1007/3-540-28962-3_19

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-22954-4

  • Online ISBN: 978-3-540-28962-3

  • eBook Packages: MedicineMedicine (R0)

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