Analysis for antithrombin gene polymorphisms in Japanese subjects and cosegregation studies in families with hereditary antithrombin deficiency-Reference-Cited by-同舟云学术

Analysis for antithrombin gene polymorphisms in Japanese subjects and cosegregation studies in families with hereditary antithrombin deficiency

Published:1996-05 Issue:3 Volume:82 Page:275-280
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Yamazaki Tomio,Katsumi Akira,Tsuzuki Shinobu,Sugiura Isamu,Kojima Tetsuhito,Takamatsu Junki,Saito Hidehiko

Publisher

Elsevier BV

Subject

Hematology

Reference14 articles.

1. Antithrombin III Toyama; replacement of Arginine 47 by Cysteine in hereditary abnormal antithrombin III that lacks heparin-binding ability;Koide,1984

2. Congenital antithrombin III deficiency (AT-III Kyoto): identification of a point mutation altering arginine-406 to methionine behind the reactive site;Nakagawa;Thromb Res,1991

3. Two new nonsense mutations in type Ia antithrombin III deficiency at Leu 140 and Arg 197;Tomonari;Thromb Haemost,1992

4. Antithrombin III mutation database: first update;Lane;Thromb Haemost,1993

5. Complete nucleotide sequence of the antithrombin gene. Evidence for homozygous recombination causing thrombophilia;Olds;Biochemistry,1993

Cited by 2 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. Antithrombin III Deficiency in Indian Patients with Deep Vein Thrombosis: Identification of First India Based AT Variants Including a Novel Point Mutation (T280A) that Leads to Aggregation;PLOS ONE;2015-03-26

2. Polymorphisms in factor V and antithrombin III gene in recurrent pregnancy loss: a case–control study in Indian population;Journal of Thrombosis and Thrombolysis;2015-03-14