Molecular basis of the clotting defect in a bleeding patient missing the Asp-185 codon in the factor X gene
Author:
Funder
National Heart, Lung, and Blood Institute of the National Institutes of Health
Publisher
Elsevier BV
Subject
Hematology
Reference27 articles.
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1. Genotypes and phenotypes characterization of 17 Iranian patients with inherited factor X deficiency: identification of a novel mutation: Leu487Phe;Blood Coagulation & Fibrinolysis;2022-03
2. Characterization of a Missense Mutation in the Catalytic Domain and a Splicing Mutation of Coagulation Factor X Compound Heterozygous in a Chinese Pedigree;Genes;2021-09-27
3. A Compound Heterozygosis of Two Novel Mutations Causes Factor X Deficiency in a Chinese Pedigree;Acta Haematologica;2020-06-29
4. The Disulfide Bond between Cys22 and Cys27 in the Protease Domain Modulate Clotting Activity of Coagulation Factor X;Thrombosis and Haemostasis;2019-03-27
5. The biochemistry of blister fluid from pediatric burn injuries: proteomics and metabolomics aspects;Expert Review of Proteomics;2015-12-19
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