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Thromb Haemost 1998; 80(04): 709-710
DOI: 10.1055/s-0037-1615451
DOI: 10.1055/s-0037-1615451
Letters to the Editor
Factors X Nice I and II: Two Novel Missense Mutations (Met-40Val and Pro304Ser) in Patient with Coagulation Factor X Deficiency
Further Information
Publication History
Received
15 January 1998
Accepted after resubmission
29 June 1998
Publication Date:
08 December 2017 (online)
![](https://www.thieme-connect.de/media/10.1055-s-00035024/199804/lookinside/thumbnails/10-1055-s-0037-1615451-1.jpg)
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References
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- 3 Miao CH, Leytus SP, Chung DW, Davie EW. Liver-specific expression of the gene coding for human factor X, a blood coagulation factor.. J Biol Chem 1992; 267: 7395-401.
- 4 Cooper DN, Millar DS, Wacey A, Pemberton S, Tuddenham EGD. Inherited factor X deficiency: Molecular genetics and pathophysiology.. Thromb Haemost 1998; 78: 161-72.
- 5 Scambler PJ, Williamson R. The structural gene for human coagulation factor X is located on chromosome 13q34.. Cytogenet Cell Genet 1985; 39: 231-3.
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- 7 Miyata T, Kojima T, Suzuki K, Umeyama H, Yamazaki T, Kamiya T, Toyoda H, Kato H. Factor X Nagoya 1 and Nagoya 2: A CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively.. Thromb Haemost 1998; 79: 486-90.
- 8 Padmanabhan K, Padmanabhan KP, Tulinsky A, Park CH, Bode W, Huber R, Blankenship DT, Cardin AD, Kisiel W. Structure of human des(1-45) factor Xa at 2.2 Å resolution.. J Mol Biol 1993; 232: 947-66.