Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.02759.x/fullpdf
Reference36 articles.
1. Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations;Attali;Thrombosis and Haemostasis,1999
2. Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies;Becker;American Journal of Human Genetics,1996
3. A new MspI restriction fragment length polymorphism in the hemophilia B locus;Camerino;Human Genetics,1985
4. CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series;Chen;Human Genetics,1991
5. The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions;Cooper;Human Genetics,1990
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