Gene therapy: towards a one-time cure for β-thalassemia
Thalassemia is a highly prevalent monogenic inherited hemolytic disease in southern China, typically caused by defects in the β-globin gene or α-globin gene that disrupt hemoglobin synthesis. China has over 30 million carriers of thalassemia genes, among whom about 300, 000 are patients with severe...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Chinês |
| Publicado em: |
Editorial Office of Journal of Guangxi Medical University
2025-10-01
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| coleção: | Guangxi Yike Daxue xuebao |
| Assuntos: | |
| Acesso em linha: | https://journal.gxmu.edu.cn/article/doi/10.16190/j.cnki.45-1211/r.2025.05.001 |
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