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Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia

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Summary

The molecular heterogeneity of GPI deficiency is demonstrated. All variants studied are different from each other. The clinical picture is characterized by nonspherocytic hemolytic anemia.

Zusammenfassung

Die molekulare Heterogenität des Glucosephosphat-Isomerase-Mangels wird beschrieben. Alle untersuchten Varianten sind voneinander verschieden. Das klinische Bild ist durch eine nichtsphärozytäre hämolytische Anämie gekennzeichnet.

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References

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Author notes

  1. Georg W. Löhr

    Present address: Medizinische Universitätsklinik Freiburg/Brsg., 78, Freiburg/Brsg., BRD

Authors and Affiliations

  1. Medizinische Universitätsklinik Freiburg/Brsg., 78, Freiburg/Brsg., BRD

    Heidwolf Arnold, Karl G. Blume, Rupert Engelhardt & Ernst Beutler

  2. City of Hope National Medical Center, Duarte, California, USA

    Georg W. Löhr, Heidwolf Arnold, Karl G. Blume, Rupert Engelhardt & Ernst Beutler

Authors
  1. Georg W. Löhr
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  2. Heidwolf Arnold
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  3. Karl G. Blume
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  4. Rupert Engelhardt
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  5. Ernst Beutler
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Löhr, G.W., Arnold, H., Blume, K.G. et al. Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia. Blut 26, 393–398 (1973). https://doi.org/10.1007/BF01632749

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  • DOI: https://doi.org/10.1007/BF01632749

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