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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation

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Journal of Inherited Metabolic Disease

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References

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Authors and Affiliations

  1. Department of Paediatrics, University Hospital Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands

    R. J. A. Wanders, L. Ijlst & A. H. van Gennip

  2. Department of Paediatrics, Free University Amsterdam, de Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands

    C. Jakobs

  3. Department of Paediatrics, Streekziekenhuis Helmond-Deurne, The Netherlands

    J. P. de Jager

  4. University Children's Hospital ‘Het Wilhelmina Kinderziekenhuis’, Nieuwegracht 137, 3512 LK, Utrecht, The Netherlands

    L. Dorland, F. J. van Sprang & M. Duran

Authors
  1. R. J. A. Wanders
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  2. L. Ijlst
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  3. A. H. van Gennip
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  4. C. Jakobs
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  5. J. P. de Jager
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  6. L. Dorland
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  7. F. J. van Sprang
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  8. M. Duran
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Wanders, R.J.A., Ijlst, L., van Gennip, A.H. et al. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation. J Inherit Metab Dis 13, 311–314 (1990). https://doi.org/10.1007/BF01799383

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  • DOI: https://doi.org/10.1007/BF01799383

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