Structural interpretation of 42 mutations causing factor XI deficiency using homology modeling
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2004.01088.x/fullpdf
Reference79 articles.
1. Roles of Platelets and Factor XI in the Initiation of Blood Coagulation by Thrombin
2. Definition of the Bleeding Tendency in Factor XI-Deficient Kindreds–A Clinical and Laboratory Study
3. Organization of the gene for human factor XI
4. Amino acid sequence of human factor XI, a blood coagulation factor with four tandem repeats that are highly homologous with plasma prekallikrein
5. Domains of invasion organelle proteins from apicomplexan parasites are homologous with the Apple domains of blood coagulation factor XI and plasma pre-kallikrein and are members of the PAN module superfamily
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3. Molecular analysis in 12 factor XI deficiency patients from China: Identification of three novel splicing mutations;Thrombosis Research;2020-08
4. Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations;International Journal of Hematology;2020-04-24
5. Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype–phenotype relationship;Human Genome Variation;2017-11-09
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