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Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran

Background: Xmn-1 polymorphism of 𝜸(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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Detalles Bibliográficos
Autores principales:	Miri-Moghaddam, Ebrahim, Bahrami, Sara, Naderi, Majid, Bazi, Ali, Karimipoor, Morteza
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575729/ https://www.ncbi.nlm.nih.gov/pubmed/28875012

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