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Novel Βeta (β)-Thalassemia Mutation in Turkish Children
Beta (β)-thalassemia is the most frequently observed hereditary blood disorder in the world. It is characterized by deficiency of hemoglobin β-globin gene and is also a profoundly heterogeneous both at the molecular and clinical level. In the case of β-thalassemia, there is reduced (β(+) type) or ab...
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| 出版年: | Indian J Hematol Blood Transfus |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer India
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4375154/ https://ncbi.nlm.nih.gov/pubmed/25825561 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-014-0380-6 |
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