Race, ethnicity, F8 variants, and inhibitor risk: analysis of the “My Life Our Future” hemophilia A database
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference59 articles.
1. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A;Lakich;Nat Genet,1993
2. Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions;Naylor;Hum Mol Genet,1993
3. A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels;Viel;Blood,2007
4. Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative;Johnsen;Blood Adv,2017
5. My Life Our Future programme. Genotypes, phenotypes and whole genome sequence: Approaches from the My Life Our Future haemophilia project;Konkle;Haemophilia,2018
Cited by 5 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. Race and ethnicity and the success of immune tolerance induction among people with severe haemophilia A in the United States;Haemophilia;2024-03-10
2. Recent Advances in Genetic and Non-Genetic Factors Related to the Development of Hemophilia Inhibitors;Advances in Clinical Medicine;2024
3. Race, ethnicity, and immune tolerance induction in hemophilia A in the United States;Research and Practice in Thrombosis and Haemostasis;2023-11
4. Corrigendum to ‘Race, ethnicity, F8 variants and inhibitor risk: Analysis of the “My Life Our Future” Hemophilia A database’ [Journal of Thrombosis and Haemostasis Volume 21, Issue 4, April 2023, Pages 800-813];Journal of Thrombosis and Haemostasis;2023-06
5. Anti-FVIII antibodies in Black and White hemophilia A subjects: do F8 haplotypes play a role?;Blood Advances;2022-12-02
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