An A to T transversion at position −5 of the Factor IX promoter results in hemophilia B
- 31 January 1992
- Vol. 12 (1), 161-163
- https://doi.org/10.1016/0888-7543(92)90421-n
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- A less severe form of Haemophilia B LeydenNucleic Acids Research, 1990
- A past mutation at Isoleucine397 is now a common cause of moderate/mild haemophilia BBritish Journal of Haematology, 1990
- Disruption of a C/EBP binding site in the factor IX promoter is associated with haemophilia BNature, 1990
- Haemophilia B: database of point mutations and short additions and deletionsNucleic Acids Research, 1990
- Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype)Blood, 1989
- The putative factor IX gene promoter in hemophilia B LeydenBlood, 1988
- Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia BBritish Journal of Haematology, 1986
- Complete nucleotide sequences of the gene for human factor IX (antihemophilic factor B)Biochemistry, 1985
- Hemophilia B LeydenNew England Journal of Medicine, 1982