Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations
Author:
Affiliation:
1. Department of Genetics Faculty of Advanced Sciences and Technology Islamic Azad University of Medical Sciences Tehran Iran
2. Human Genetic Research Center Baqiyatallah University of Medical Sciences Tehran Iran
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.3294
Reference49 articles.
1. Factor IX deficiency (Christmas disease)
2. Eighteen Years of Molecular Genotyping the Hemophilia Inversion Hotspot: From Southern Blot to Inverse Shifting-PCR
3. A study of intron 22 inversion type I and II of coagulation factor 8 gene in patients with severe Hemophilia A using IS‐PCR technique;Rouzafzay N;Qom Univ Med Sci J,2008
4. Evaluation of a chromogenic factor VIII assay on the Sysmex CS 2100i instrument;Kloppers JF;Med Technol SA
5. Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A
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