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Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand.

Hemoglobin - 1 May 2020

Panyasai Sitthichai, Pornprasert Sakorn

Abstract excerpt

In this study, Hb A2 variants and their association with α- and β-thalassemia (α- and β-thal) were analyzed. We performed molecular analyses to identify α-thal [- -SEA (Southeast Asian), - -THAI (Thai), -α3.7 (rightward) and -α4.2 (leftward)] deletions, and Hb Constant Spring (Hb CS; HBA2: c.427T>C), Hb A2-Melbourne (HBD: c.130G>A), Hb A2' (HBD: c.49G>C), Hb A2-Lampang (HBD: c.142G>A). β0-Thalassemia mutations...

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Identifiers

PMID: 32482156
DOI: 10.1080/03630269.2020.1770099

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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