Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual-Reference-Cited by-同舟云学术

Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual

Published:2021-07-19 Issue:3 Volume:2 Page:366-374
ISSN:2688-6146
Container-title:eJHaem
language:en
Short-container-title:eJHaem

Author:

Hamid Mohammad¹^ORCID,keikhaei Bijan²,Galehdari Hamid³,Saberi Alihossein⁴,Sedaghat Alireza⁵,Shariati Gholamreza⁴⁶,Mohammadi‐Anaei Marziye⁶

Affiliation:

1. Department of Molecular Medicine, Biotechnology Research Center Pasteur Institute of Iran Tehran Iran

2. Research Center for Thalassemia and Hemoglobinopathy, Health Institute Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

3. Department of Genetics, Faculty of Sciences Shahid Chamran University of Ahvaz Ahvaz Iran

4. Department of Medical Genetics, Faculty of Medicine Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

5. Department of Endocrinology Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran

6. Narges Medical Genetics and PND Laboratory Ahvaz Iran

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jha2.262

Reference36 articles.

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3. Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia

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5. Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?

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3. Hematological and genetic profiles of persons with co‐inherited heterozygous β‐thalassemia and supernumerary α‐globin genes;European Journal of Haematology;2023-01-14

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