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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...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Indian J Hematol Blood Transfus
Päätekijät: Kumar, Ravindra, Kaur, Anupriya, Agarwal, Sarita
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer India 2013
Aiheet:
Linkit: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
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