Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A

Author:

Bi L.,Lawler A.M.,Antonarakis S.E.,High K.A.,Gearhart J.D.,Kazazian H.H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference28 articles.

1. Rizza, C.R. & Spooner, R.J.D. Treatment of haemophilia and related disorders in Britain and Northern Ireland during 1976–1980: Report on behalf of the Directors of Haemophilia Centres in the United Kingdom. Br. med. J. 286, 391–402 (1983).

2. Sadler, J.E. & Davie, E.W. Haemophilia A, haemophilia B and von Willebrand's disease. in The Molecular Basis of Blood Disease. (eds Stamatoyanopoulos, G. et al.) 575–630 (W.B. Saunders, Philadelphia, 1987).

3. Kazazian, H.H. Jr., Tuddenham, E.G.D. & Antonarakis, S.E. Haemophilia A and parahaemophilia: deficiencies of factors VIII and V. in Medical and Metabolic Basis of Inherited Disease, 7th edn (eds Scriver, C. et al.) 3241–3267 (McGraw-Hill, New York, 1995).

4. Graham, J.B. & Brinkhous, K.M. Canine and equine haemophillia, in Hand book of Haemophilia (eds Graham, J.B. et.al) (Elsevier, New York, 1975).

5. Evans, J.P. et al. Canine haemophilia B resulting from a point mutation with unusual consequences. Proc. natn. Acad. Sci. U.S.A. 86, 10095–10099 (1989).

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