Evidence that descendants of three founders constitute about 25% of hemophilia B in the united states
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference12 articles.
1. A past mutation of isoleucine 397 is now a common cause of moderate/mild hemophilia B;Bottema;Br. J. Haematol,1990
2. Hemophilia B Durham: A mutation in the first EGF-like domain of factor IX that is characterized by polymerase chain reaction;Denton;Blood,1988
3. The Pennsylvania hemophilia program 1973–1978;Eyster;Am. J. Hematol,1980
4. Haemophilia B: Database of point mutations and short additions and deletions;Giannelli;Nucleic Acids Res,1990
5. The incidence and distribution of CpG → TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots;Green;Nucleic Acids Res,1990
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