Literature DB >> 14717992

The factor VIII gene intron 1 inversion mutation: prevalence in severe hemophilia A patients in the UK.

A M Cumming.   

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Year:  2004        PMID： 14717992     DOI： 10.1111/j.1538-7836.2004.0562i.x

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


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  4 in total

1.  Severe hemophilia A in a Japanese female caused by an F8-intron 22 inversion associated with skewed X chromosome inactivation.

Authors:  Yuhri Miyawaki; Atsuo Suzuki; Yuhta Fujimori; Akira Takagi; Takashi Murate; Nobuaki Suzuki; Akira Katsumi; Tomoki Naoe; Koji Yamamoto; Tadashi Matsushita; Junki Takamatsu; Tetsuhito Kojima
Journal:  Int J Hematol       Date:  2010-08-11       Impact factor: 2.490

2.  Genotyping of Intron Inversions and Point Mutations in Exon 14 of the FVIII Gene in Iranian Azeri Turkish Families with Hemophilia A.

Authors:  Mahmoud Shekari Khaniani; Abdollah Ebrahimi; Setareh Daraei; Sima Mansoori Derakhshan
Journal:  Indian J Hematol Blood Transfus       Date:  2016-06-27       Impact factor: 0.900

3.  Gene Expression Modification by an Autosomal Inversion Associated With Three Male Mating Morphs.

Authors:  Jasmine L Loveland; David B Lank; Clemens Küpper
Journal:  Front Genet       Date:  2021-06-04       Impact factor: 4.599

4.  Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China.

Authors:  Yin Feng; Qianqian Li; Panlai Shi; Ning Liu; Xiangdong Kong; Ruixia Guo
Journal:  Haemophilia       Date:  2020-11-27       Impact factor: 4.287
  4 in total

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