The mutation in Japanese congenital factor VII deficiency
Author:
Affiliation:
1. Department of Biomedical Laboratory Sciences, School of Health Sciences, Shinshu University
Publisher
Japanese Society on Thrombosis and Hemostasis
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjsth/19/1/19_1_64/_pdf
Reference57 articles.
1. 1) Williams WJ, Ernest B, A llan JE, Marshall AL : Hematology. 3rd ed. New York, McGraw-Hill, 1983, 1393-1394.
2. 2) Alexiander B, Goldstein R, Landwehr G, Cook CD : Congential SPCA deficiency : A hitherto unreconized coagulation defect with hemorrhage recified by serum and serum fractions. J Clin Invest 30 : 596-608, 1951.
3. 5) Takamiya O, Kinoshita S, Yoshioka K : Electroimmunoassay of Factor VII antigen. Thromb Res 42 : 847-853, 1986.
4. 6) Takamiya O, Funahashi S, Kinoshita S, Yoshioka A, Yoshioka K, Ikawa H : Factor VII activity and antigen in a factor VII abnormality. J. Lab & Clin. Haematol 10 : 159-165, 1988.
5. 7) McVey JH, Boswell E, Mumford AD, Kemball-Cook G, Tuddenham EG : Factor VII deficiency and the FVII mutation database. Hum Mutat 17 : 3-17, 2001.
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Congenital Factor VII Deficiency with Bleeding after Surgery for Advanced Gastric Cancer;The Japanese Journal of Gastroenterological Surgery;2019-06-01
2. Compound heterozygous mutations (p.Leu13Pro and p.Tyr294*) associated with factor VII deficiency cause impaired secretion through ineffective translocation and extensive intracellular degradation of factor VII;Thrombosis Research;2013-02
3. Factor VII Deficiency due to Compound Heterozygosity for Leu-48Pro Mutation and a Novel Pro260Leu Mutation;Clinical and Applied Thrombosis/Hemostasis;2011-03-24
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