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Analysis of the Haematological Phenotype and Molecular Characteristics of Rare Abnormal Haemoglobin.

Molecular genetics & genomic medicine - 1 Sept 2024

Ge Yanfen, Zheng Guansheng, Xian Luhua, Luo Yanfei, Liu Junru, Lin Ting, Cui Wenhao, Yang Yujing, Shan Huizhuang

Abstract excerpt

BACKGROUND: Haemoglobinopathy refers to a group of common monogenic inherited conditions associated with variations in the haemoglobin molecule; however, there is relatively limited reporting on abnormal haemoglobinopathy in the Chinese population, especially rare abnormal haemoglobin (Hb). The aim of this study was to explore the clinical characteristics of haemoglobinopathy to supplement data for the...

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Identifiers

PMID: 39262298
DOI: 10.1002/mgg3.70012
PMCID: PMC11391098

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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