Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2010.04095.x/fullpdf
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3. Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16;Fregin;Blood,2002
4. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2;Rost;Nature,2004
5. Identification of the gene for vitamin K epoxide reductase;Li;Nature,2004
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