Molecular Mechanisms of Hemoglobin F Induction

Molecular Mechanisms of Hemoglobin F Induction

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Hemoglobin F (HbF, α2γ2) is a major contributor to the clinical heterogeneity and ameliorating agent observed in patients with the β-globin disorders including β-thalassemia and sickle cell disease (SCD). During fetal life, HbF is the major hemoglobin but is lar...

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Bibliographic Details
Main Authors:	Najmaldin Saki, Ali Dehghani Fard, Majid Farshdousti Hagh, Mohammad Shahjahani, Saied Kaviani
Format:	Article
Language:	English
Published:	Tehran University of Medical Sciences 2011-10-01
Series:	International Journal of Hematology-Oncology and Stem Cell Research
Subjects:	Hemoglobin F β-thalassemia Expression Induction
Online Access:	http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/20851.pdf&manuscript_id=20851

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