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

Surada Satthakarna Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Phayao Province, Thailand; View further author information

Sasis Boonmeeb Department of Medical Technology, Maesot Hospital, Tak, Tak Province, ThailandView further author information

Sitthichai Panyasaia Department of Medical Technology, School of Allied Health Sciences, University of Phayao, Phayao, Phayao Province, Thailand; Correspondence[email protected]

https://orcid.org/0000-0002-7589-3849 View further author information

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Juan Liao, Qin Li, Li-Qin Ling, Chao-Nan Liu, Xun-Bei Huang & Jing Zhou. (2022) 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 46:4, pages 249-252.
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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

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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

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