A novel point mutation in severe haemophilia A: a further proof of genotype-phenotype correlation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2009.02153.x/fullpdf
Reference4 articles.
1. The tertiary structure and domain organization of coagulation factor VIII;Shen;Blood,2008
2. Synthetic factor VIII peptides with aminoacid sequences contained within the C2 domain of factor VIII inhibit factor VIII binding to phosphatidyl serine;Foster;Blood,1990
3. Laboratory methods for the genetic diagnosis of bleeding disorders;Goodeve;Clin Lab Haematol,1998
4. Molecular characterization of severe haemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene;Higuchi;Proc Natl Acad Sci USA,1991
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