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Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran
Background: Xmn-1 polymorphism of (G)globin gene (HBG2) is a prominent quantitative trait loci (QTL) in β-thalassemia intermediate (β-TI). In current study, we evaluated the frequency of Xmn-1 polymorphism and its association with β-globin gene (HBB) alleles and Hb F level in β-TI patients in Sista...
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| Yayımlandı: | Int J Hematol Oncol Stem Cell Res |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5575729/ https://ncbi.nlm.nih.gov/pubmed/28875012 |
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