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Coagulation Factor XIII Mutation Profile: Update 2004

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35th Hemophilia Symposium

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References

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  2. Ichinose A. Physiopathology and regulation of factor XIII. Thromb Haemost 2001 Jul; 86(1): 57–65

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  3. Takahashi N, Tsukamoto H, Umeyama H, Castaman G, Rodeghiero F, Ichinose A. Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression system. Blood 1998 Apr 15; 91(8): 2830–8

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Authors
  1. V. Ivaskevicius
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  2. R. Seitz
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  3. H.-H. Brackmann
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  4. W. Eberl
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  5. K. Kurnik
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  6. W. Kreuz
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  7. R. Klamroth
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  8. H. Rott
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  9. R. M. Loreth
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  10. F. Herrmann
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  11. E. Seifried
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  12. J. Oldenburg
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Editor information

Editors and Affiliations

  1. Hemophilia Center, Dept. of Internal Medicine, University Hospital, Theodor-Stern-Kai 7, D-60590, Frankfurt am Main, Germany

    Inge Scharrer

  2. Dept. of Hemostaseology, University Hospital, Ziemssenstr. 1a, D-80336, München, Germany

    Wolfgang Schramm

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© 2006 Springer Verlag Berlin Heidelberg

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Ivaskevicius, V. et al. (2006). Coagulation Factor XIII Mutation Profile: Update 2004. In: Scharrer, I., Schramm, W. (eds) 35th Hemophilia Symposium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-28546-6_50

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  • DOI: https://doi.org/10.1007/3-540-28546-6_50

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-28543-4

  • Online ISBN: 978-3-540-28546-5

  • eBook Packages: MedicineMedicine (R0)

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