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Diamond-Blackfan anemia with very late and fatal onset aplasia in a 55-year-old patient with RPL11 mutation

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References

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Funding

The authors received no funding for this case report.

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Authors and Affiliations

  1. Institute of Clinical Chemistry and Laboratory Medicine, Hospital Wels-Grieskirchen, Grieskirchnerstraße 42, Wels, 4600, Austria

    Bernhard Strasser & Alexander Haushofer

  2. Institute of Internal Medicine IV, Hospital Wels-Grieskirchen, Wels, Austria

    Sonja Heibl

  3. Munich Leukemia Laboratory, Munich, Germany

    Gregor Hörmann

Authors
  1. Bernhard Strasser
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  2. Sonja Heibl
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  3. Gregor Hörmann
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  4. Alexander Haushofer
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Contributions

All authors contributed to the study conception and design. The first draft of the manuscript was written by Bernhard Strasser and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript and agree to be accountable for all aspects of the work.

Corresponding author

Correspondence to Bernhard Strasser.

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The authors declare that they have no competing interest.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Informed consent was obtained from all individual participants included in the study.

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Strasser, B., Heibl, S., Hörmann, G. et al. Diamond-Blackfan anemia with very late and fatal onset aplasia in a 55-year-old patient with RPL11 mutation. Ann Hematol 103, 1011–1012 (2024). https://doi.org/10.1007/s00277-023-05553-3

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  • DOI: https://doi.org/10.1007/s00277-023-05553-3

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