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The molecular genetics of antithrombin deficiency.

作者信息

Olds R J, Lane D A, Thein S L

机构信息

Institute of Molecular Medicine, John Radcliffe Hospital, Oxford.

出版信息

Br J Haematol. 1994 Jun;87(2):221-6. doi: 10.1111/j.1365-2141.1994.tb04902.x.

DOI:10.1111/j.1365-2141.1994.tb04902.x
PMID:7947262
Abstract
摘要

相似文献

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Antithrombin-TRI (Ala382 to Thr) causing severe thromboembolic tendency undergoes the S-to-R transition and is associated with a plasma-inactive high-molecular-weight complex of aggregated antithrombin.导致严重血栓栓塞倾向的抗凝血酶-TRI（丙氨酸382突变为苏氨酸）发生了从S型到R型的转变，并与聚集的抗凝血酶的血浆非活性高分子量复合物有关。
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引用本文的文献

1
Guidelines for the management of thrombophilia. Department of Haematology, The Royal London Hospital, Whitechapel, London, UK.血栓形成倾向管理指南。英国伦敦白教堂区皇家伦敦医院血液科
Postgrad Med J. 1996 Feb;72(844):87-94. doi: 10.1136/pgmj.72.844.87.
2
Antithrombin III: summary of first database update.抗凝血酶III：首个数据库更新总结
Nucleic Acids Res. 1994 Sep;22(17):3556-9.