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A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: Relation of organic aciduria to phenotype?

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Journal of Inherited Metabolic Disease

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References

  • Goodman, S. I. and Frerman, F. E. Organic acidemias due to defects in lysine oxidation. 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. 845–855

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  • Przyrembel, H. Defects of lysine degradation. In Fernandes, J., Saudubray, J. M. and Tada, K. (eds.)Inborn Metabolic Diseases: Diagnosis and Treatment, Springer-Verlag, Berlin, 1990, pp. 301–311

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Authors and Affiliations

  1. Department of Pediatrics, Free University Hospital, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands

    C. Jakobs & A. J. C. de Grauw

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  1. C. Jakobs
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  2. A. J. C. de Grauw
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Jakobs, C., de Grauw, A.J.C. A fatal case of 2-keto-, 2-hydroxy- and 2-aminoadipic aciduria: Relation of organic aciduria to phenotype?. J Inherit Metab Dis 15, 279–280 (1992). https://doi.org/10.1007/BF01799643

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  • DOI: https://doi.org/10.1007/BF01799643

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