[Analysis of five Chinese individuals with rare thalassemia mutation HBB: c.93-21G＞A].
The hematological phenotype of β-thalassemia carriers (HBB: c.93-21G＞A) is similar to that of other β<sup>+</sup> thalassemia heterozygotes with mild β-thalassemia characteristics.
Authors
- Guang-Kuan Zeng
- Li‐Ye Yang (ORCID: https://orcid.org/0000-0003-1581-9089)
- Xiaomin Ma (ORCID: https://orcid.org/0009-0006-0458-5132)
- Yuchan Huang
- Xiaohua Yu (ORCID: https://orcid.org/0000-0002-0233-0121)
- Lili Liu (ORCID: https://orcid.org/0000-0002-8073-8309)
- Yan-Bin Cao
- Yuwei Liao (ORCID: https://orcid.org/0000-0001-8248-0359)
- Jianlian Liang
- Yiyuan Ge
- Bairu Lai
- Yan-Qing Zeng (ORCID: https://orcid.org/0009-0008-7345-670X)
Institutions
- Qujiang People's Hospital (CN)
- People's Hospital of Yangzhong (CN)
Publication Details
- Journal
- PubMed
- Published
- 2024-10-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-20240108-00015
- Citations
- 1
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article