Identification of two novel β-globin gene mutations HBB: exon3del, HBB: c.−81A>C
ABSTRACTBackground β-thalassemia is a common inherited hemolytic disorder caused by mutations in the HBB gene. Genetic analysis of 2 new beta-thalassemia patients with deletion mutations in the HBB gene and their family members.Methods Their clinical presentation and blood phenotypic tests were anal...
محفوظ في:
| المؤلفون الرئيسيون: | , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Taylor & Francis Group
2023-12-01
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| سلاسل: | Hematology |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://www.tandfonline.com/doi/10.1080/16078454.2023.2265723 |
| الوسوم: |
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