Literature DB >> 16194213

Characterization of a novel prothrombin variant, Prothrombin C20209T, as a modifier of thrombotic risk among African-Americans.

H Itakura, M J Telen, C C Hoppe, D A E White, J L Zehnder.   

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Year:  2005        PMID： 16194213     DOI： 10.1111/j.1538-7836.2005.01562.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN： 1538-7836            Impact factor:   5.824


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  3 in total

Review 1.  A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes I: general principles and overview.

Authors:  Jian-Min Chen; Claude Férec; David N Cooper
Journal:  Hum Genet       Date:  2006-04-28       Impact factor: 4.132

2.  Prothrombin C20209T mutation in deep vein thrombosis: a case report.

Authors:  Mariela Muñoz; Cristian Vilos; Mario Cantín
Journal:  Int J Clin Exp Med       Date:  2015-07-15

3.  A deep vein thrombosis caused by 20209C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient.

Authors:  Silvia Izquierdo Alvarez; Eva Barrio Ollero; Francisco Miguel Llinares Sanjuan; Fabiola Lorente Martínez; María Teresa Calvo Martín
Journal:  Biochem Med (Zagreb)       Date:  2014-02-15       Impact factor: 2.313
  3 in total

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