Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology,General Medicine
Reference29 articles.
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1. Gene Variants in Two Families with Inherited Coagulation Factor XI Deficiency and Identification of Mutations;Acta Haematologica;2022-12-21
2. A Common Missense Variant Causing Factor XI Deficiency and Increased Bleeding Tendency in Maine Coon Cats;Genes;2022-04-28
3. A novel mutation (Tyr503Cys) in a severe factor XI deficiency;Blood Coagulation & Fibrinolysis;2018-04
4. Cys482Trp Missense Mutation in the Coagulation Factor XI Gene (F11) in a Korean Patient with Factor XI Deficiency;Annals of Laboratory Medicine;2014-07-01
5. A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15;Blood Coagulation & Fibrinolysis;2014-03
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