Krüppel-Like Factor 1Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia-Reference-Cited by-同舟云学术

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Krüppel-Like Factor 1Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia

Published:2019-01-02 Issue:1 Volume:43 Page:12-17
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Tamaddoni Ahmad¹,Khabaz Astaneh Sahar²,Tabaripour Reza²,Akhavan-Niaki Haleh³

Affiliation:

1. Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran;

2. Department of Cellular and Molecular Biology, Islamic Azad University, Babol Branch, Babol, Iran;

3. Department of Genetics, Faculty of Medicine, Babol University of Medical Sciences, Babol, Iran

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1567528

Reference36 articles.

1. A KLF1 gene mutation causes β-thalassemia minor in a Chinese family

2. Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

3. A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population

Cited by 3 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. Erythroid Krüppel-Like Factor (KLF1): A Surprisingly Versatile Regulator of Erythroid Differentiation;Advances in Experimental Medicine and Biology;2024

2. Mutation in thalassemia syndrome and clinical manifestation;Immunopathologia Persa;2020-06-01

3. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

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