Literature DB >> 17461935

Atypical mutations of the prothrombin gene at positions 20,209 and 20,218, and a novel mutation at position 20,219. Report on 10 patients.

C Flaujac, J Conard, M H Horellou, L Le Flem, M M Samama.   

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Year:  2007        PMID： 17461935     DOI： 10.1111/j.1538-7836.2007.02478.x

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


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  3 in total

1.  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

2.  The 3' end prothrombin gene variants in serbian patients with idiopathic thrombophilia.

Authors:  M Aradjanski; V Djordjevic; I Pruner; B Tomic; M Gvozdenov; M Kovac; D Radojkovic
Journal:  Balkan J Med Genet       Date:  2015-04-10       Impact factor: 0.519

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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