Profiling of factor VIII mutations in Korean haemophilia A
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2009.02086.x/fullpdf
Reference22 articles.
1. Mutating factor VIII: lessons from structure to function;Fay;Blood Rev,2005
2. Haemophilia A: from mutation analysis to new therapies;Graw;Nature Rev,2005
3. Haemophilia A and haemophilia B: molecular insights;Bowen;Mol Pathol,2002
4. The life cycle of coagulation factor VIII in view of its structure and function;Lenting;Blood,1998
5. The relationship of N-linked glycosylation and heavy chain-binding protein association with the secretion of glycoproteins;Dorner;J Cell Biol,1987
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1. Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations;Clinical Case Reports;2020-09-15
2. Restoration of FVIII expression by targeted gene insertion in the FVIII locus in hemophilia A patient-derived iPSCs;Experimental & Molecular Medicine;2019-04
3. Hemophilia A in a Female Patient with Recurrent Vitreous Hemorrhage;Journal of the Korean Ophthalmological Society;2019
4. The activity of factor VIII and IX of cord blood at mid-trimester in fetuses without hemophilia;Journal of Genetic Medicine;2016-12-31
5. Genotyping of Intron Inversions and Point Mutations in Exon 14 of the FVIII Gene in Iranian Azeri Turkish Families with Hemophilia A;Indian Journal of Hematology and Blood Transfusion;2016-06-27
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