The rare hemoglobin variants Hb O-Arab and Hb D-Punjab identified in population-based genetic screening throughout Guangxi, China

BackgroundHemoglobinopathies are a group of autosomal recessive disorders characterized by a high degree of clinical and genetic heterogeneity. Comprehensive genetic screening for hemoglobin variants is crucial for prevention and treatment of these conditions. Single-molecule real-time (SMRT) sequen...

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Bibliographic Details
Main Authors: Chunrong Gui, Zifeng Cheng, Yongsheng Chen, Yunting Ma, Hongfei Chen, Wei Wei, Xianda Wei, Juliang Liu, Xu Zhou, Qianqian Du, Yinghui Lai, Baoheng Gui
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Genetics
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Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2025.1622391/full
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