Molecular basis of antithrombin deficiency in four Japanese patients with antithrombin gene abnormalities including two novel mutations-Reference-Cited by-同舟云学术

Molecular basis of antithrombin deficiency in four Japanese patients with antithrombin gene abnormalities including two novel mutations

Published:2007 Issue:8 Volume:82 Page:702-705
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Kyotani Mayu,Okumura Kaoru,Takagi Akira,Murate Takashi,Yamamoto Koji,Matsushita Tadashi,Sugimura Motoi,Kanayama Naohiro,Kobayashi Takao,Saito Hidehiko,Kojima Tetsuhito

Publisher

Wiley

Subject

Hematology

Reference16 articles.

1. Biochemistry of heparin antithrombin interactions, and the physiologic role of this natural anticoagulant mechanism

2. Complete nucleotide sequence of the antithrombin gene: Evidence for homologous recombination causing thrombophilia

3. The anticoagulant activation of antithrombin by heparin

4. Antithrombin: The Principal Inhibitor of Thrombin

5. Congenital antithrombin III deficiency: insights into the pathogenesis of the hypercoagulable state and its management using markers of hemostatic system activation

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