Literature DB >> 15735818

High frequency of premature termination mutations in the factor V gene: three factor V deficiency case reports and a mutation review.

Iris Schrijver1, Debbie W Hong, Lisa Mandle, Carol D Jones, Donna DiMichele, Paul E Monahan, James L Zehnder.   

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Year:  2005        PMID： 15735818

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


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  2 in total

1.  Molecular genetic analysis for the para-Bombay blood group revealing two novel alleles in the FUT1 gene.

Authors:  Xiao-Hong Cai; Sha Jin; Xi Liu; Liang-Feng Fan; Qiong Lu; Dong Xiang
Journal:  Blood Transfus       Date:  2011-06-15       Impact factor: 3.443

2.  Identification of four novel mutations in F5 associated with congenital factor V deficiency.

Authors:  Sachiko Kanaji; Taisuke Kanaji; Miho Honda; Sachie Nakazato; Kazuo Wakayama; Yoshitomi Tabata; Shoichiro Shibata; Hisashi Gondo; Ikuko Nakamura; Koichi Node; Masanori Miura; Masaharu Miyahara; Takashi Okamura; Fumio Nagumo; Shoichiro Ohta; Kenji Izuhara
Journal:  Int J Hematol       Date:  2008-12-04       Impact factor: 2.490
  2 in total

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