Study on Hb H disease caused by the α2-globin gene initiation codon ATG > GTG mutation combined with Southeast Asian deletional α-thalassemia
Objective To explore the hemoglobin H (Hb H) diseases diseases caused by a rare α2-globin gene mutation combined with the Southeast Asian deletion of α -thalassemia gene mutation. Methods For the suspected cases of Hb H disease screened in the First Affiliated Hospital of Guangxi Medical University...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | Chinese |
| Published: |
Editorial Office of Journal of Guangxi Medical University
2025-06-01
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| Series: | Guangxi Yike Daxue xuebao |
| Subjects: | |
| Online Access: | https://journal.gxmu.edu.cn/article/doi/10.16190/j.cnki.45-1211/r.2025.03.012 |
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