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Bleeding Tendency in Factor XI Deficiency: Report on two Families and the Detection of a Novel Mutation within the Factor XI Gene

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34th Hemophilia Symposium

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References

  1. Bolton-Maggs PHB, Patterson DK, Wensley RT, Tuddenham EGD (1995) Definition of the bleeding tendency in factor XI — deficient kindreds — a clinical and laboratory study. Thromb Haemostas 73: 194–2002

    CAS  Google Scholar 

  2. HAMSTeRS: http: // europium.csc.mrc.ac.uk

    Google Scholar 

  3. Maak B, Bergmann F, Kochhan L, Estel Ch (2003) Factor XI deficiency caused by a hitherto unknown mutation in the factor XI gene. Scharrer I, Schramm W (Ed.) 32nd Hemophilia Symposium Hamburg 2001, Springer-Verlag Berlin Heidelberg, p. 203–210.

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  4. Mc Vey JH, Imanaka Y, Nishimura T, O’Brien DP, Bolton-Maggs PHB, Tuddenham EGD (1995) Identification of a novel mechanism of human genetic disease: a missense mutation causing factor XI deficiency through a change in mRNA stability. Thromb Haemostas 73:1442

    Google Scholar 

  5. Peter MK, Meili EO, von Felten A (1995) Factor XI deficiency: additional hemostatic defects are present in patients with bleeding tendency. Thromb Haemostas 73: 1442

    Google Scholar 

  6. Seligsohn U (1993) Factor XI deficiency. Thromb Haemostas 70: 68–71

    CAS  Google Scholar 

  7. Tavori S, Brenner B, Tatarsky I (1990) The effect of combined factor XI deficiency with von Willebrand factor abnormalities on haemorrhagic diathesis. Thromb Haemostas 63: 36–38

    CAS  Google Scholar 

  8. Uen C, Klopp N, Oldenburg I, Brackmann HH, Schramm W, Schwaab R, Graw I (2003) 11 novel mutations in the factor VIII encoding gene lead to severe or moderate hemophilia A. Scharrer I, Schramm W (Ed) 32nd Hemophilia Symposium Hamburg 2001, Springer-Verlag Berlin-Heidelberg, p 25–31.

    Google Scholar 

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© 2005 Springer Medizin Verlag Heidelberg

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Maak, B. et al. (2005). Bleeding Tendency in Factor XI Deficiency: Report on two Families and the Detection of a Novel Mutation within the Factor XI Gene. In: Scharrer, I., Schramm, W. (eds) 34th Hemophilia Symposium. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-27022-1_25

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  • DOI: https://doi.org/10.1007/3-540-27022-1_25

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-22886-8

  • Online ISBN: 978-3-540-27022-5

  • eBook Packages: MedicineMedicine (R0)

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