Literature DB >> 20015217

Characterization of the genetic basis of FXI deficiency in two Turkish patients.

E Berber, V Rimoldi, S Usluer, S Aksu, Y Pekcelen, S H Cağlayan, S Duga.   

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Year:  2009        PMID： 20015217     DOI： 10.1111/j.1365-2516.2009.02152.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


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  3 in total

1.  Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.

Authors:  Suar Çakı Kılıç; F Dilara İçağasıoğlu; A Sami Güven; Ergül Berber
Journal:  Blood Transfus       Date:  2014-07       Impact factor: 3.443

2.  Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.

Authors:  Seyma Colakoglu; Turan Bayhan; Betül Tavil; Ebru Yılmaz Keskin; Volkan Cakir; Fatma Gümrük; Mualla Çetin; Selin Aytaç; Ergul Berber
Journal:  Blood Transfus       Date:  2016-10-04       Impact factor: 3.443

3.  [A family with hereditary FⅪ deficiency caused by compound heterozygous mutation].

Authors:  X Y Zheng; Y H Jin; Y Y Xu; L L Yang; L Q Zhu; H H Wang; S T Jiang; M S Wang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2021-08-14
  3 in total

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