Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population-Reference-Cited by-同舟云学术

Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population

Published:2020-07-03 Issue:4 Volume:44 Page:225-230
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Hamid Mohammad¹,Zargan Nezhad Ebtesam²,Keikhaei Bijan³,Galehdari Hamid⁴,Saberi Alihossein⁴,Sedaghat Alireza⁵,Mohammadi-Anaei Marziye⁶,Shariati Gholamreza⁴⁶

Affiliation:

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

2. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

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

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

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

6. Narges Medical Genetics Laboratory, Kianpars, Ahvaz, Iran

Funder

Pasteur Institute of Iran, Tehran

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1790384

Reference24 articles.

1. The Molecular Basis of -Thalassemia

2. HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB Gene

3. The Prevention of Thalassemia

4. Disorders of Hemoglobin

5. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies

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. Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene;Archives of Iranian Medicine;2022-05-01

2. T2-weighted cardiovascular magnetic resonance and echocardiographic arterial elasticity criteria for monitoring cardiac siderosis in patients with beta-thalassemia major;Journal of Research in Medical Sciences;2022