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Clinical correlation of dysequilibrium syndrome and 4-hydroxybutyric aciduria

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Journal of Inherited Metabolic Disease

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References

  • Gibson, K. M., Sweetman, L., Nyhan, W. L., Lenoir, G. and Divry, P. Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduria.Eur. J. Pediatr. 142 (1984) 257–259

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  • Rating, D., Hanefeld, F., Siemes, H., Jakobs, C., Kneer, J., Hermier, M. and Divry, P. 4-Hydroxybutyric aciduria. A new inborn error of metabolism. I. Clinical review.J. Inher. Metab. Dis. 7, Suppl. 1 (1982) 90–92

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  • Schurig, V., Van Orman, A. and Bowen, P. Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites.Am. J. Med. Genet. 9 (1981) 45–35

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Authors and Affiliations

  1. Department of Pediatrics, University of California, San Diego, La Jolla, California, USA

    K. M. Gibson, L. Sweetman & W. L. Nyhan

  2. Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada

    P. Bowen

Authors
  1. K. M. Gibson
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  2. L. Sweetman
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  3. W. L. Nyhan
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  4. P. Bowen
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Gibson, K.M., Sweetman, L., Nyhan, W.L. et al. Clinical correlation of dysequilibrium syndrome and 4-hydroxybutyric aciduria. J Inherit Metab Dis 8, 58 (1985). https://doi.org/10.1007/BF01801664

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  • DOI: https://doi.org/10.1007/BF01801664

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