The factor VIII gene intron 1 inversion mutation: prevalence in severe hemophilia A patients in the UK
- 9 January 2004
- journal article
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 2 (1) , 192-206
- https://doi.org/10.1111/j.1538-7836.2004.0562i.x
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia ABlood, 2002
- Two chimaeric transcription units result from an inversion breaking intron 1 of the factor VIII gene and a region reportedly affected by reciprocal translocations in T-cell leukaemiaHuman Molecular Genetics, 1996
- Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyBlood, 1995
- Inversions disrupting the factor VIII gene are a common cause of severe haemophilia ANature Genetics, 1993