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Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia.

Hemoglobin - 1 May 2020

Jiang Fan, Ju Ai-Ping, Li Jian, Chen Gui-Lan, Zhou Jian-Ying, Tang Xue-Wei, Zuo Lian-Dong, Li Dong-Zhi

Abstract excerpt

Hb Westmead (α122(H5)His>Gln) (HBA2: c.369C>G) is a common α-globin variant causing α-thalassemia (α-thal) in Mainland China. In this study, we report the hematological characteristics in Hb Westmead carriers in a Chinese population. There were 546 individuals carrying Hb Westmead based on their molecular diagnosis: 514 Hb Westmead heterozygotes and 32 compound heterozygotes for Hb Westmead and α0-thal. Compared...

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Identifiers

PMID: 32436451
DOI: 10.1080/03630269.2020.1768109

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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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