Hematologic features of beta-globin gene mutation type (?o) with homozygous beta thalassemia
β-Tthalassemia is common genetic disorders in Turkey that characterized by the reduced synthesis (β+) or absence (βo) of the β-globin chains in the HbA molecule. In this study, we aimed to determine the effect of the mutation type of the β-globin gene on hematological values in homozygous β-thalasse...
Furkejuvvon:
| Váldodahkkit: | , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
National Academy of Sciences of Ukraine, Palladin Institute of Biochemistry
2018-07-01
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| Ráidu: | The Ukrainian Biochemical Journal |
| Fáttát: | |
| Liŋkkat: | http://ukrbiochemjournal.org/wp-content/uploads/2018/06/Özbolat_4_18.pdf |
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