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Biochemical and nutritional status of children with hyperphenylalaninaemia

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Journal of Inherited Metabolic Disease

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References

  • Manz, F., Schmidt, H., Scharer, K. and Bickel, H. Acid-base status in dietary treatment of phenylketonuria.Pediatr. Res. 11 (1977) 1084

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  • O'Flynn, M. E., Holtzman, N. A., Blaskovics, M., Azen, C. and Williamson, M. L. The diagnosis of phenylketonuria.Am. J. Dis. Child. 134 (1980) 769–774

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Authors and Affiliations

  1. Department of Pediatrics, University of Colorado School of Medicine, 80262, Denver, Colorado, USA

    A. M. Nord, L. McCabe & E. R. B. McCabe

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  1. A. M. Nord
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  2. L. McCabe
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  3. E. R. B. McCabe
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Nord, A.M., McCabe, L. & McCabe, E.R.B. Biochemical and nutritional status of children with hyperphenylalaninaemia. J Inherit Metab Dis 11, 431–432 (1988). https://doi.org/10.1007/BF01800437

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  • DOI: https://doi.org/10.1007/BF01800437

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