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Sialuria: a follow-up report

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Gahl, W. A., Renlund, M. and Thoene, J. G. Lysosomal transport disorders. In Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.)The Metabolic Basis of Inherited Disease, 6th edn. McGraw Hill, New York, 1989, pp. 2640–2641

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  • Seppala, R., Tietze, F., Weiss, P., Ashwell, G., Barsh, G. and Gahl, W. A. The metabolic defect in sialuria: lack of feedback control of uridine disphosphateN-acetylglucosamine 2-epimerase.Am. J. Hum. Genet. 45 (Suppl. 1) (1989) A11

  • Wilcken, B., Don, N., Greenaway, R., Hammond, J. and Sosula, L. Sialuria: A second case.J. Inher. Metab. Dis. 10 (1987) 97–99

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Authors and Affiliations

  1. The Oliver Latham Laboratory and the Children's Hospital, Camperdown, The St. George Hospital, Sydney, Australia

    N. A. Don &  B. Wilcken

Authors
  1. N. A. Don
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  2. B. Wilcken
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Don, N.A., Wilcken, B. Sialuria: a follow-up report. J Inherit Metab Dis 14, 942 (1991). https://doi.org/10.1007/BF01800480

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  • DOI: https://doi.org/10.1007/BF01800480

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