Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2-Reference-Cited by-同舟云学术

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Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2

Published:2019-01-02 Issue:1 Volume:43 Page:52-55
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Nuinoon Manit¹^ORCID,Thipthara Orapan²,Fucharoen Suthat³

Affiliation:

1. School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand;

2. Department of Pediatrics, Maharaj Nakhon Si Thammarat Hospital, Nakhon Si Thammarat, Thailand;

3. Thalassemia Research Center, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom, Thailand

Funder

Thailand Research Fund

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1599907

Reference22 articles.

1. 1 The population genetics of the haemoglobinopathies

2. Clinical Manifestation of β-Thalassemia/Hemoglobin E Disease

3. Clinical and hematologic aspects of hemoglobin E β-thalassemia

4. Genetic Factors Affecting Clinical Severity in β-Thalassemia Syndromes

5. A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E

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. Genome Sequencing Technology used to Explore the 6mA Methylation Level of Silent Alpha-Thalassemia in Postmenopausal Women;Clinical Laboratory;2020

2. Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βCD121(−G) (HBB:c.364delG) in exon 3 of β-globin gene;Journal of Clinical Pathology;2019-12-26

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