Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients-Reference-Cited by-同舟云学术

Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients

Published:2016-11-17 Issue:3 Volume:105 Page:287-294
ISSN:0925-5710
Container-title:International Journal of Hematology
language:en
Short-container-title:Int J Hematol

Author:

Sekiya Akiko^ORCID,Taniguchi Fumina,Yamaguchi Daisuke,Kamijima Sayaka,Kaneko Shonosuke,Katsu Shiori,Hanamura Miho,Takata Mao,Nakano Haruka,Asakura Hidesaku,Ohtake Shigeki,Morishita Eriko

Funder

Ministry of Health, Labour and Welfare

Japan Society for the Promotion of Science

Hokkoku Cancer Fund

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Link

http://link.springer.com/content/pdf/10.1007/s12185-016-2142-8.pdf

Reference30 articles.

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2. Jin L, Abrahams JP, Skinner R, Petitou M, Pike RN, Carrell RW. The anticoagulant activation of antithrombin by heparin. Proc Natl Acad Sci USA. 1997;94(26):14683–8.

3. Olson ST, Bjork I, Bock SC. Identification of critical molecular interactions mediating heparin activation of antithrombin: implications for the design of improved heparin anticoagulants. Trends Cardiovasc Med. 2002;12(5):198–205.

4. Luxembourg B, Delev D, Geisen C, Spannagl M, Krause M, Miesbach W, et al. Molecular basis of antithrombin deficiency. Thromb Haemost. 2011;105(4):635–46.

5. Lane D, Kunz G, Olds RJ, Thein SL. Molecular genetics of antithrombin deficiency. Blood Rev. 1996;10(2):59–74.

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