References
- Vehar GA, Keyt B, Eaton D, Rodriguez H, O'Brien DP, Rotblat F, Oppermann H, Keck R, Wood WI, Harkins RN, et al. Structure of human factor VIII. Nature 1984; 312(5992): 337-342.
- Balton-Maggs PH, Pasi KJ. Haemophilias A and B. Lancet 2003; 361(9371): 1801-1809.
- Bagnall RD, Waseem N, Green PM, Giannelli F. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe Hemophilia A. Blood 2002; 99(1):168-174.
- Eyster ME, Lewis JH, Shapiro SS, Gill F, Kajani M, Prager D, Djerassi I, Rice S, Lusch C, Keller A. The Pennsylvania hemophilia program 1973-78. Am J Hematol 1980; 9(3): 277-286.
- Miller SA, Dykes DD, Polesky HF. A simple salting-out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16(3):1215.
- Salviato R, Belvini D, Radossi P, Tagariello G. Factor VIII gene intron 1 inversion: lower than expected prevalence in Italian haemophiliac severe patients. Haemophilia 2004; 10(2): 194-196.
- Andrikovics H, Klein I, Bors A, Nemes L, Marosi A, Varadi A, Tordai A. Analysis of large structural changes of factor VIII gene, involving intron 1 and 22, in severe haemophilia A. Haemotologica 2003; 88(7): 778-784.
- Habart D, Kalabova D, Hrachovinova I, Vorlova Z. Significant prevalence of the intron 1 factor VIII gene inversion among patients with severe Hemophilia A in the Czech Republic. J Thromb Haemost 2003; 1(4): 1323-1324.
- Cumming AM. UK Haemophilia Centre Doctors' Organization Haemophilia Genetics Laboratory Network. The factor VIII gene intron 1 inversion mutation: prevalence in severe Haemophilia A patients in the UK. J Thromb Haemost 2004; 2(1): 205-206.
- Rastegar Lari G, Enayat MS, Arzang Z, Laverne JM, Ala, F. Identification of intron 1 and 22 inversion mutations in the factor VIII gene of 124 Iranian families with severe Haemophilia A. Haemophilia 2004; 10(4):410-411.
- Ghosh K, Shetty S and Mohanty D. Inversion of intron 1 is a rare cause of severe Hemophilia A in Indian population. J Thromb Haemost 2004; 2(8): 1481-1482.