The factor VIII gene intron 1 inversion mutation: prevalence in severe hemophilia A patients in the UK
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2004.0562i.x/fullpdf
Reference7 articles.
1. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A
2. Factor VIII gene inversions in severe hemophilia A: results of an international consortium study
3. Two chimaeric transcription units result from an inversion breaking intron 1 of the factor VIII gene and a region reportedly affected by reciprocal translocations in T-cell leukaemia
4. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A
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1. An integrated multitool analysis contributes elements to interpreting unclassified factor IX missense variants associated with hemophilia B;Journal of Thrombosis and Haemostasis;2024-07
2. Large Intron Inversions in Romanian Patients with Hemophilia A—First Report;Medicina;2023-10-13
3. Harmonization of Hemostasis Testing Across a Large Laboratory Network: An Example from Australia;Methods in Molecular Biology;2023
4. Gene Expression Modification by an Autosomal Inversion Associated With Three Male Mating Morphs;Frontiers in Genetics;2021-06-04
5. Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients;Molecular Genetics & Genomic Medicine;2020-12-20
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