A point mutation (Arg271→Cys) of a homozygote for dysfunctional prothrombin, prothrombin Obihiro, which has a region of high sequence variability
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1995.tb05601.x/fullpdf
Reference15 articles.
1. Nucleotide sequence of the gene for human prothrombin
2. Molecular defects of factor IX Chicago-2 (Arg 145----His) and prothrombin Madrid (Arg 271----cys): arginine mutations that preclude zymogen activation
3. Identification of the primary structural defect in the dysthrombin thrombin Quick I: substitution of cysteine for arginine-382
4. Substitution of valine for glycine-558 in the congenital dysthrombin thrombin Quick II alters primary substrate specificity
5. Ncol RFLP in the human prothrombin (F2) gene
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