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Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Davidson-Mundt A, Luder AS, Greene CL (1992) Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency. J Pediatr 120: 444–446.

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  • Treem WR, Witzleben CA, Piccoli DA et al (1986) Medium-chain and long-chain acyl-CoA dehydrogenase deficiency: clinical, pathologic, and ultrastructural differentiation from Reye's syndrome. Hepatology 6: 1270–1278.

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Authors and Affiliations

  1. Division of Metabolic Diseases, University Children's Hospital, Heidelberg, Germany

    E. Mayatepek

  2. University Children's Hospital, Münster, Germany

    H. G. Koch

  3. Department of Neuropediatrics and Metabolic Diseases, University Children's Hospital, Marburg, Germany

    G. F. Hoffmann

Authors
  1. E. Mayatepek
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  2. H. G. Koch
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  3. G. F. Hoffmann
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Mayatepek, E., Koch, H.G. & Hoffmann, G.F. Hyperuricaemia and medium-chain acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 20, 842–843 (1997). https://doi.org/10.1023/A:1005300708445

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  • DOI: https://doi.org/10.1023/A:1005300708445

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