Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients-Reference-Cited by-同舟云学术

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Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients

Published:2020-03-03 Issue:2 Volume:44 Page:109-112
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Azarkeivan Azita¹,Cohan Nader²,Niazkar Hamid Reza³,Azizi Arsalan⁴,Rad Fariba⁴^ORCID

Affiliation:

1. Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran;

2. Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran;

3. Student Research Committee, Gonabad University of Medical Sciences, Gonabad, Iran;

4. Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1757462

Reference25 articles.

1. Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on theHBA1Gene

2. First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain

3. Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration

4. PREVALENCE OF ß-THALASSEMIA MUTATIONS AMONG NORTHEASTERN IRANIAN POPULATION AND THEIR IMPACTS ON HEMATOLOGICAL INDICES AND APPLICATION OF PRENATAL DIAGNOSIS, A SEVEN-YEARS STUDY

Cited by 1 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. Serum Zinc Level in β-Thalassemia Major: A Retrospective Study in Southwest Iran;Hemoglobin;2021-04-26

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