Congenital factor XI deficiency, complete genotype and phenotype of two Iranian families-Reference-Cited by-同舟云学术

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Congenital factor XI deficiency, complete genotype and phenotype of two Iranian families

Published:2019-12 Issue:8 Volume:30 Page:409-412
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Dorgalaleh Akbar,Gholaminezhad Masoume,Shiravand Yavar,Naderi Majid,Safa Majid

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference15 articles.

1. The role of factor XI in coagulation: a matter of revision;Minnema;Semin Thromb Hemost,1999

2. An update on factor XI structure and function;Mohammed;Thromb Res,2017

3. Organization of the gene for human factor XI;Asakai;Biochemistry,1987

4. Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4;Kato;Cytogenet Cell Genet,1989

5. Congenital factor XI deficiency: an update;Duga;Semin Thromb Hemost,2013

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Molecular basis of rare congenital bleeding disorders;Blood Reviews;2023-05

2. Gene Variants in Two Families with Inherited Coagulation Factor XI Deficiency and Identification of Mutations;Acta Haematologica;2022-12-21

3. Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency;Blood Coagulation & Fibrinolysis;2021-11-16

4. Phenotype and genotype analysis of patients with severe factor XI deficiency in Shaanxi Province, China;Blood Coagulation & Fibrinolysis;2021-07-08

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