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Article

Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family.

Hemoglobin - 1 Jan 2017

He Sheng, Qin Qian, Lin Li, Chen Qiuli, Yi Shang, Wei Honhwei, Du Juan, Zheng Chenguang, Qiu Xiaoxia, Chen Biyan

Abstract excerpt

Hb Q-Thailand [α74(EF3)Asp→His (α1); HBA1: c.223 G>C] is an abnormal hemoglobin (Hb), variant found mainly in China and Southeast Asian countries. The association of the αQ-Thailand allele with other globin gene disorders has important implications in diagnosis. Here, we report a hitherto undescribed condition of patients with a double heterozygosity for Hb Q-Thailand with α0-thalassemia (α0-thal) and in...

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Source

Identifiers

PMID: 28475397
DOI: 10.1080/03630269.2017.1295985

Genes

HBA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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