A Genetic Variant of Factor IX with Decreased Capacity for Ca2+Binding
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1979.tb01175.x/fullpdf
Reference24 articles.
1. Prothrombin fragments. Ca2+ binding and activation kinetics.
2. Inhibitor-neutralisation assay and electro-immuno assay of human factor IX (Christmas factor)
3. The Abnormal Factor IX of Hemophilia B+ Variants
4. The Levels of Factors II, VII, IX and X by Antibody Neutralization Techniques in the Plasma of Patients Receiving Phenindione Therapy
5. The gamma-carboxy glutamic acid content of human and bovine prothrombin following warfarin treatment
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1. Factor IX Zutphen: a Cys18→Arg mutation results in formation of a heterodimer with α1-microglobulin and the inability to form a calcium-induced conformation;Biochemical Journal;1995-11-01
2. Identification of haemophilia B patients with mutations in the two calcium binding domains of factor IX: importance of a β-OH Asp 64→Asn change;British Journal of Haematology;1991-01
3. A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia Bm;British Journal of Haematology;1990-06
4. Carrier detection in the hemophilias;American Journal of Hematology;1987-11
5. Protein S Deficiency Occurs in the Nephrotic Syndrome;Annals of Internal Medicine;1987-07-01
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