Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran-Reference-Cited by-同舟云学术

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Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the α2-Globin Gene Expanding the Genetic Spectrum of α-Thalassemia in Iran

Published:2020-10-14 Issue:6 Volume:44 Page:423-426
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Forouzesh Pour Fatemeh¹,Karimi Keyvan¹,Ghaderi Zhila¹,Tavakoli Koudehi Ameneh¹,Najmabadi Hossein¹²

Affiliation:

1. Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran

2. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1831529

Reference21 articles.

1. Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran

2. Elucidating the spectrum of -thalassemia mutations in Iran

3. Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience

4. A novel polyadenylation signal mutation in the α2-globin gene causing α thalassaemia

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene;Hemoglobin;2022-11-02

2. Characterization of a novel HBB:c.194dup variant of the β-globin gene combined with six alpha genes;Journal of International Medical Research;2022-05

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