Literature DB >> 15613050

First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene.

L Hilbert, R D'Oiron, E Fressinaud, D Meyer, C Mazurier.   

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Year:  2004        PMID： 15613050     DOI： 10.1111/j.1538-7836.2004.01049.x

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


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  3 in total

1.  The von Willebrand factor D'D3 assembly and structural principles for factor VIII binding and concatemer biogenesis.

Authors:  Xianchi Dong; Nina C Leksa; Ekta Seth Chhabra; Joseph W Arndt; Qi Lu; Kevin E Knockenhauer; Robert T Peters; Timothy A Springer
Journal:  Blood       Date:  2019-01-14       Impact factor: 22.113

Review 2.  New insight into the molecular basis of hemophilia A.

Authors:  Johannes Oldenburg; Osman El-Maarri
Journal:  Int J Hematol       Date:  2006-02       Impact factor: 2.490

Review 3.  The molecular genetics of von Willebrand disease.

Authors:  Ergül Berber
Journal:  Turk J Haematol       Date:  2012-12-05       Impact factor: 1.831
  3 in total

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