• Bajaj, S.P., Rapaport, S.I. & Brown, S.F. (1981) Isolation and characterization of human factor VII: activation of factor VII by factor Xa. Journal of Biological Chemistry, 256, 253259.
  • Banner, D.W., D'Arcy, A., Chene, C., Winkler, F.K., Guha, A., Konigsberg, W.H., Nemerson, Y. & Kirchhofer, D. (1996) The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor. Nature, 380, 4146.
  • Bauer, K.A., Kass, B.L., Ten Cate, H., Hawiger, J.J. & Rosenberg, R.D. (1990) Factor IX is activated in vivo by the tissue factor mechanism. Blood, 76, 731736.
  • Bottema, C.D., Ketterling, R.P., Yoon, H.S. & Sommer, S.S. (1990) The pattern of factor IX germ-line mutation in Asians is similar to that of Caucasians. American Journal of Human Genetics, 47, 835841.
  • Carew, J.A., Pollak, E.S., High, K.A. & Bauer, K.A. (1998) Severe factor VII deficiency due to a mutation disrupting an Sp1 binding site in the factor VII promoter. Blood, 92, 16391645.
  • Fair, D.S. (1983) Quantitation of factor VII in the plasma of normal and warfarin-treated individuals by radioimmunoassay. Blood, 62, 784791.
  • Giannelli, F., Green, P.M., Sommer, S.S., Poon, M., Ludwig, M., Schwaab, R., Reitsma, P.H., Goossens, M., Yoshioka, A., Figueiredo, M.S. & Brownlee, G.G. (1998) Haemophilia B: database of point mutations and short additions and deletions-eights edition. Nucleic Acids Research, 26, 265268.
  • Green, F., Kelleher, C., Wilkes, H., Temple, A., Meade, T. & Humphries, S. (1991) A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals. Arteriosclerosis and Thrombosis, 11, 540546.
  • Greenberg, D., Miao, C.H., Ho, W.T., Chung, D.W. & Davie, E.W. (1995) Liver-specific expression of the human factor VII gene. Proceedings of the National Academy of Sciences of the United States of America, 92, 1234712351.
  • Hagen, F.S., Gray, C.L., O'Hara, P., Grant, F.J., Saari, G.C., Woodbury, R.G., Hart, C.E., Insley, M., Kisiel, W., Kurachi, K. & Davie, E.W. (1986) Characterization of a cDNA coding for human factor VII. Proceedings of the National Academy of Sciences of the United States of America, 83, 24122416.
  • Van't Hooft, F.M., Silveira, A., Tornvall, P., Iliadou, A., Ehrenborg, E., Eriksson, P. & Hamsten, A. (1999) Two common functional polymorphisms in the promoter region of the coagulation factor VII gene determining plasma factor VII activity and mass concentration. Blood, 93, 34323441.
  • Katsumi, A., Matsushita, T., Yamazaki, T., Sugiura, I., Kojima, T. & Saito, H. (2000) Severe factor VII deficiency caused by a novel mutation His348 to Gln in the catalytic domain. Thrombosis and Haemostasis, 83, 239243.
  • McVey, J.H., Boswell, E.J., Takamiya, O., Tamagnini, G., Valente, V., Fidalgo, T., Layton, M. & Tuddenham, E.G. (1998) Exclusion of the first EGF domain of factor VII by a splice site mutation causes lethal factor VII deficiency. Blood, 92, 920926.
  • Marchetti, G., Patracchini, P., Papacchini, M., Ferrati, M. & Bernardi, F. (1993) A polymorphism in the 5′ region of coagulation factor VII gene (F7) caused by an inserted decanucleotide. Human Genetics, 90, 575576.
  • Nagaizumi, K., Inaba, H., Itho, T., Yamanaka, K., Suzuki, T., Nishida, Y., Hagiwara, T., Amano, K., Kagawa, K., Arai, M. & Fukutake, K. (2001) Identification of missense mutations in the FVII gene of three FVII deficiencies. Japanese Journal of Thrombosis and Haemostasis, 12, 133143.
  • Nobauer-Huhmann, I.M., Holler, W., Krinninger, B., Turecek, P.L., Richter, G., Scharrer, I., Forberg, E. & Watzke, H.H. (1998) Factor X Frankfurt I: molecular and functional characterization of a hereditary factor X deficiency (Gla25Lys). Blood Coagulation and Fibrinolysis, 9, 143152.
  • O'Hara, P.J. & Grant, F.J. (1988) The human factor VII gene is polymorphic due to variation in repeat copy number in a minisatellite. Gene, 66, 147158.
  • O'Hara, P.J., Grant, F.J., Haldeman, B.A., Gray, C.L., Insley, M.Y., Hagen, F.S. & Murray, M.J. (1987) Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation. Proceedings of the National Academy of Sciences of the United States of America, 84, 51585162.
  • Odom, M.W., Leone, G., De Stefano, V., Montiel, M.M., Boland, E.J., Anderson, J. & Jagadeeswaran, P. (1994) Five novel point mutations: two causing haemophilia B and three causing factor X deficiency. Molecular and Cellular Probes, 8, 6365.
  • Pollak, E.S., Hung, H.L., Godin, W., Overton, G.C. & High, K.A. (1996) Functional characterization of the human factor VII5′-flanking region. Journal of Biological Chemistry, 271, 17381747.
  • Reitsma, P.H., Bernardi, F., Doig, R.G., Gandrille, S., Greengard, J.S., Ireland, H., Krawczak, M., Lind, B., Long, G.L., Poort, S.R., Saito, H., Sala, N. & Witt, I. (1995) Protein C deficiency: a database of mutations, 1995 update. Thrombosis and Haemostasis, 73, 876889.
  • Tartary, M., Vidaud, D., Piao, Y., Costa, J.M., Bahnak, B.R., Fressinaud, E., Congard, B., Laurian, Y., Meyer, D. & Lavergne, J.M. (1993) Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresis. British Journal of Haematology, 84, 662669.
  • Triplett, D.A., Brandt, J.T., Batard, M.A., Dixon, J.L. & Fair, D.S. (1985) Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysis. Blood, 66, 12841287.
  • Wingender, E., Dietze, P., Karas, H. & Knuppel, R. (1996) TRANSFAC: a database on transcription factors and their DNA binding sites. Nucleic Acids Research, 24, 238241.