Hb SKMC and an unprecedented γδβ-thalassemia: first report from Iraq
Background Thalassemias are genetic disorders of globin chain synthesis. In Iraq, β-thalassemia is more prevalent than α-thalassemia. This study identifies two unpredicted globin gene mutations, a rare α-globin gene mutation (Hb SKMC) and a novel γδβ-thalassemia deletion.Methods Over 2 years, the Ge...
Furkejuvvon:
| Váldodahkkit: | , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Taylor & Francis Group
2024-12-01
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| Ráidu: | Hematology |
| Fáttát: | |
| Liŋkkat: | https://www.tandfonline.com/doi/10.1080/16078454.2024.2399356 |
| Fáddágilkorat: |
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