A novel homozygous missense mutation in the factor VII gene of severe factor VII deficiency in a pedigree: a description of two cases
Author:
Affiliation:
1. Department of Hematology; Qingdao Municipal Hospital; Qingdao City; 266071; Shandong Province; China
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12176/fullpdf
Reference7 articles.
1. Factor VII Deficiency;Mariani;Semin Thromb Hemost,2009
2. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene;Herrmann;Haemophilia,2009
3. Identification of genetic defects underlying FVII deficiency in 10 patients belonging to eight unrelated families of the North provinces from Tunisia;Elmahmoudi;Diagn Pathol,2012
4. Molecular characterisation and three dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency;Peyvandi;Thromb Haemost,2000
5. Factor VII deficiency;Perry;Br J Haematol,2002
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