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Decreased activity of respiratory-chain enzymes in glutaric aciduria type II

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Journal of Inherited Metabolic Disease

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References

  • Scholte HR, Ross JD, Blom W et al (1992) Assessment of deficiencies of fatty acyl-CoA dehydrogenases in fibroblasts, muscle and liver.J Inher Metab Dis 15: 347–352.

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  • Scholte HR, de Klerk JBC, Boonman AMC et al (1993) Respiratory chain disorders in tissues of a patient who died from glutaric aciduria type II.Enzyme Protein 47: 9.

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

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Authors and Affiliations

  1. Department of Pediatrics, University of Kiel, Schwanenweg 20, D-24105, Kiel, Germany

    R. Santer, A. Claaβ, M. Krawinkel & J. Schaub

  2. Department of Pediatrics, University of Nijmegen, PO Box 9101, NL-6500, Nijmegen, The Netherlands

    W. Ruitenbeek

Authors
  1. R. Santer
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  2. A. Claaβ
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  3. M. Krawinkel
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  4. J. Schaub
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  5. W. Ruitenbeek
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Santer, R., Claaβ, A., Krawinkel, M. et al. Decreased activity of respiratory-chain enzymes in glutaric aciduria type II. J Inherit Metab Dis 18, 75–76 (1995). https://doi.org/10.1007/BF00711377

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  • DOI: https://doi.org/10.1007/BF00711377

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