Literature DB >> 9798997

A polymorphism nt 1628G-->A (R485K) in exon 10 of the coagulation factor V gene may be a risk factor for thrombosis in the indigenous Thai population.

M Hiyoshi, P Arnutti, W Prayoonwiwat, O Nathalang, C Suwanasophon, R Kokaseam, S Hashimoto, T Takubo, S Tagawa, M Fukui, N Tatsumi.   

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Year:  1998        PMID： 9798997

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  3 in total

1.  Functional polymorphisms of FGA, encoding alpha fibrinogen, are associated with susceptibility to venous thromboembolism in a Taiwanese population.

Authors:  Yu-Lin Ko; Lung-An Hsu; Tsu-Shiu Hsu; Chia-Ti Tsai; Ming-Sheng Teng; Semon Wu; Chi-Jen Chang; Ying-Shiung Lee
Journal:  Hum Genet       Date:  2005-12-14       Impact factor: 4.132

2.  Single nucleotide polymorphisms other than factor V Leiden are associated with coagulopathy and osteonecrosis of the femoral head in Chinese patients.

Authors:  Kou-Ti Peng; Kuo-Chin Huang; Tsan-Wen Huang; Yun-Shien Lee; Wei-Hsiu Hsu; Robert W W Hsu; Steve W N Ueng; Mel S Lee
Journal:  PLoS One       Date:  2014-08-13       Impact factor: 3.240

3.  Targeted next-generation resequencing of f5 gene identifies novel multiple variants pattern in severe hereditary factor v deficiency.

Authors:  Piotr K Janicki; Sonia Vaida; Hamid A B Al-Mondhiry
Journal:  Case Rep Genet       Date:  2013-04-15
  3 in total

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