Art
J-GLOBAL ID：200902135505604835
Reference number：95A0957184
Identification of the antithrombin III Kyoto mutation by restriction fragment length polymorphism analysis.
制限断片長多形分析によるアンチトロンビンIIIKyoto変異の同定
Author (7)：
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Material：
Volume：
61
Issue：
4
Page：
197-204
Publication year：
Jun. 1995
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
原著論文
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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Semi thesaurus term：
Thesaurus term/Semi thesaurus term
Keywords indexed to the article.
All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
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JST classification (2)：
JST classification
Category name(code) classified by JST.
Hematologic diagnosis
, Hematologic diseases
Reference (22)：
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BARROWCLIFFE, T. W. Antithrombin III and heparin. Haemostasis and Thrombosis. 1987, 849-869
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PROCHOWNIK, E. V. Intron structure of the human antithrombin III gene differs from that of other members of the serine protease inhibitor superfamily. J Biol Chem. 1985, 260, 9608-9612
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BOCK, S. C. Antithrombin III Utah: proline-407 to leucine mutation in a highly conserved region near the inhibitor reactive site. Biochemistry. 1988, 27, 6171-6178
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BOCK, S. C. Assignment of the human antithrombin III structural gene to chromosome lq23-25. Cytogenet Cell Genet. 1985, 39, 67-69
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EGEBERG, O. Inherited antithrombin deficiency causing thrombophilia. Thromb Diath Haemorrh. 1965, 13, 516-530
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