Elevated Hb A<inf>2</inf> levels in a patient with a compound heterozygosity for the (β <sup>+</sup>)-31 (A > G) and (β <sup>0</sup>) Codon 17 (A > T) mutations together with a single α-globin gene

© 2015 Informa Healthcare USA, Inc. We report the molecular and hematological feature of a Thai woman who had clinical diagnosis of β-thalassemia intermedia (β-TI). Hemoglobin (Hb) high performance liquid chromatography (HPLC) analysis identified Hb A (64.4%), Hb F (12.3%) and Hb A<inf>2</i...

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Bibliographic Details
Main Authors: Sitthichai Panyasai, Kanokwan Jaiping, Sakorn Pornprasert
Format: Journal
Published: 2018
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Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84939444466&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54195
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Institution: Chiang Mai University
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