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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Neonatal manifestation at the first day of life presenting with tachypnoea

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Journal of Inherited Metabolic Disease

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References

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Authors and Affiliations

  1. Department of Pediatrics, General Hospital of Itzehoe, Germany

    C. Thiel, S. Baudach & U. Schnackenberg

  2. Emma Children's Hospital and Department of Clinical Chemistry, University of Amsterdam, The Netherlands

    P. Vreken & R. J. A. Wanders

Authors
  1. C. Thiel
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  2. S. Baudach
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  3. U. Schnackenberg
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  4. P. Vreken
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  5. R. J. A. Wanders
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Thiel, C., Baudach, S., Schnackenberg, U. et al. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Neonatal manifestation at the first day of life presenting with tachypnoea. J Inherit Metab Dis 22, 839–840 (1999). https://doi.org/10.1023/A:1005514325872

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  • DOI: https://doi.org/10.1023/A:1005514325872

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