Identification of Missense Mutations in the FVII Gene of Three FVII Deficiencies
Author:
Affiliation:
1. Department of Clinical Pathology, Tokyo Medical University
2. First Department of Internal Medicine, Nihon University, School of Medicine
Publisher
Japanese Society on Thrombosis and Hemostasis
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjsth/12/2/12_2_133/_pdf
Reference34 articles.
1. 1) Marder VJ, Shulman NR : Clinical aspect of congenital factor VII deficiency. Am J Med 37 : 182-194, 1964.
2. 2) Hagen FS, Gray CL,O'Hara P, Grant FJ, Sarri GC, Woodbury RG, Hart CE, Insley M, Kisiel W, Kurachi K, Davie EW : Characterization of a cDNA coding for human factor VII. Proc Natl Acad Sci USA 83 : 2412-2416, 1986.
3. 3) Wion KL, Kelly D, Summerfield JA, Tuddenham EGD, Lawn RM : Distribution of factor VII mRNA and antigen in human liver and other tissues. Nature 317 : 726-729, 1985.
4. 4) Fair DS : Quantitation of factor VII in the plasma of normal and warfarin-treated individual by radio immunoassay. Blood 62 : 784-791, 1983.
5. 5) Howard PR, Bovill EG, Pike J, Church WR, Tracy RP : Factor VII antigen levels in healthy blood donor population. Thromb Haemost 72 : 21-27, 1994.
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