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Influence of Xmn 1(G)γ (HBG2 c.-211 C → T) Globin Gene Polymorphism on Phenotype of Thalassemia Patients of North India
Beta (β) thalassemia is the most common single gene disorder in India. It has been reported that in patients with β-thalassemia in the presence of Xmn 1(G)γ polymorphic site the level of fetal hemoglobin (HbF) is increased thereby reducing the severity of disease. To determine the prevalence of Xmn...
Shranjeno v:
| izdano v: | Indian J Hematol Blood Transfus |
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| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer India
2013
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4243400/ https://ncbi.nlm.nih.gov/pubmed/25435729 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-013-0293-9 |
| Oznake: |
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