Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations-Reference-Cited by-同舟云学术

Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations

Published:2020-09-15 Issue:12 Volume:8 Page:2975-2984
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Nasirnejad Sola Farzaneh¹,Morovvati Saeid²,Sabetghadam Moghadam Mitra¹^ORCID,Entezari Malihe¹

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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1. Recent Advances in Genetic and Non-Genetic Factors Related to the Development of Hemophilia Inhibitors;Advances in Clinical Medicine;2024

2. Experimental validation of a predicted microRNA within human FVIII gene;MOL BIOL RES COMMUN;2021