Molecular Defects in Hemophilia B
Author:
Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4615-3698-7_8.pdf
Reference104 articles.
1. Pavlovsky A: Contribution to the pathogenesis of hemophilia. Blood 2: 185–187, 1947
2. Aggeler PM, White SG, Glendening MB, Page EW, Leake TB, Bates G: Plasma thromboplastin component (PTC) deficiency: a new disease resembling hemophilia. Proc Soc Exper Biol Med 79: 692–694, 1952
3. Schulman I, Smith CH: Hemorrhagic disease in an infant due to a deficiency of a previously undescribed clotting factor. Blood 7: 794–807, 1952
4. Biggs R, Douglas AS, Macfarlane RG, Dacie JV, Pitney WR, Merskey C, O’Brien JR: Christmas disease, a condition previously mistaken for hemophilia. Br Med J ii: 1378–1382, 1952
5. Thompson AR: Factor IX antigen by radioimmunoassay. Abnormal factor IX protein in patients on warfarin therapy and with hemophilia B. J Clin Invest 59: 900–910, 1977
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1. CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series;Human Genetics;1991-06
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