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Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease

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Journal of Inherited Metabolic Disease

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References

  • Brown GK, Scholem RD, Bankier A, Danks DM (1984) Malonyl coenzyme A decarboxylase deficiency.J Inher Metab Dis 7: 21–26.

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  • Matalon R, Michaels K, Kaul R et al (1993) Malonic aciduria and cardiomyopathy.J Inher Metab Dis 16: 571–573.

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  • Schadewaldt P, Zuschlag A, Hammen HW, Wendel U (1992) Microassay for diagnosis of malonyl-CoA decarboxylase deficiency in cells.SSIEM Annual Symposium, Abstract P165.

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Authors and Affiliations

  1. Department of Paediatrics, University of Kiel, Germany

    M. B. Krawinkel, R. Santer & J. Schaub

  2. Children's Hospital, Municipal Hospitals, Flensburg, Germany

    H. D. Oldigs

  3. Department of Paediatrics, University of Freiburg, Germany

    W. Lehnert

  4. Akademisch Ziekenhuis, Kindergeneeskunde Nijmegen, Netherlands

    U. Wendel

Authors
  1. M. B. Krawinkel
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  2. H. D. Oldigs
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  3. R. Santer
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  4. W. Lehnert
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  5. U. Wendel
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  6. J. Schaub
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Krawinkel, M.B., Oldigs, H.D., Santer, R. et al. Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease. J Inherit Metab Dis 17, 636–637 (1994). https://doi.org/10.1007/BF00711609

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  • DOI: https://doi.org/10.1007/BF00711609

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