Art
J-GLOBAL ID：200902127551589481
Reference number：01A0497636
One Missense Mutation in the Factor X Gene Causing Factor X Deficiency-Factor X Kanazawa.
第X因子欠損症を引き起こす第X因子遺伝子のミスセンス変異 第X因子Kanazawa
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Material：
Volume：
73
Issue：
3
Page：
390-392
Publication year：
Apr. 2001
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
短報
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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Semi thesaurus term：
Thesaurus term/Semi thesaurus term
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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.
JST classification (1)：
JST classification
Category name(code) classified by JST.
Hematologic diagnosis
Reference (14)：
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BAUER, K. A. Detection of factor X activation in human. Blood. 1989, 74, 2007-2015
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MESSIER, T. L. Cloning and expression in COS-1 cells of a full-length cDNA encoding human coagulation factor X. Gene. 1991, 99, 291-294
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LEYTUS, S. P. Gene for human factor X: a blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C. Biochemistry. 1986, 25, 5098-5102
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MIAO, C. H. Liver-specific expression of the gene coding for human factor X, a blood coagulation factor. J Biol Chem. 1992, 267, 7395-7401
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COOPER, D. N. Inherited factor X deficiency: molecular genetics and pathophysiology. Thromb Haemost. 1997, 78, 161-172
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