Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant-Reference-Cited by-同舟云学术

Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant

Published:2020-11-01 Issue:6 Volume:44 Page:385-390
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Satthakarn Surada¹,Boonmee Sasis²,Panyasai Sitthichai¹^ORCID

Affiliation:

1. Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Phayao Province, Thailand;

2. Department of Medical Technology, Maesot Hospital, Tak, Tak Province, Thailand

Funder

School of Allied Health Sciences, University of Phayao, Phayo, Thailand

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1848860

Reference20 articles.

1. Pathophysiology and Clinical Manifestations of the -Thalassemias

2. Molecular basis of β thalassemia and potential therapeutic targets

3. High Incidence of 3-Thalassemia, Hemoglobin E, and Glucose-6-Phosphate Dehydrogenase Deficiency in Populations of Malaria-Endemic Southern Shan State, Myanmar

4. Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia

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1. A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β⁰ Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB: c.151A>T) mutation in cis];Hemoglobin;2022-05-16