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HBG2 -158 (C>T) polymorphism and its contribution to fetal hemoglobin variability in Iraqi Kurds with beta-thalassemia minor

PURPOSE: Hemoglobin (Hb) F% is increased in up to half of beta-thalassemia (β-thal) carriers. Several polymorphisms have been linked to such variability in different populations, including HBG2 - 158(C>T) (Xmn I polymorphism) on chromosome 11. To determine the role of this polymorphism in such va...

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Detalles Bibliográficos
Autores principales:	Albarawi, Dilan J., Balatay, Amer A., Al-Allawi, Nasir
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2018
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210847/ https://www.ncbi.nlm.nih.gov/pubmed/30498305 http://dx.doi.org/10.4103/JLP.JLP_22_18

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