CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00204177.pdf
Reference33 articles.
1. Bird AP (1980) DNA methylation and the frequency of CpG in animal DNA. Nucleic Acids Res 8:1499?1504
2. Bitter K (1964) Erhebungen zur Bestimmung der Mutationsrate f�r Hamophilie A und B in Hamburg. Z Mensch Vererb Konstitutionslehre 37:251?268
3. Bottema CDK, Koeberl DD, Sommer SS (1989) Direct carrier testing in 14 families with hemophilia B. Lancet II:526?529
4. Bottema CDK, Ketterling RP, Koeberl DD, Bowie EJW, Taylor SAM, Lillicrap D, Shapiro A, Gilchrist G, Sommer SS (1990) A past mutation at isoleucine 397 now is a common cause of moderate-mild hemophilia B. Br J Haematol 75:212?216
5. Bouvier DP, Chen SH, Thompson AR (1990) A 50 bp polymorphic insertion in the factor IX gene is readily detected by amplification and is in equilibrium with other polymorphic sites. Nucleic Acids Res 18:5325
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