HbA2: biology, clinical relevance and a possible target for ameliorating sickle cell disease
Author:
Affiliation:
1. Department of Medicine; Boston University School of Medicine; Boston MA USA
2. National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; Bethesda MD USA
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.13570/fullpdf
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2. Hemoglobin Parchman: double crossover within a single human gene;Adams;Science,1982
3. Molecular mechanism of high hemoglobin F production in Southeast Asian-type hereditary persistence of fetal hemoglobin;Changsri;International Journal of Hematology,2006
4. Observations on the levels of Hb A 2 in patients with different á-thalassemia mutations and a ë chain variant;Codrington;Blood,1990
5. Activation of ë-globin gene expression by erythroid Krupple- like factor: a potential approach for gene therapy of sickle cell disease;Donze;Blood,1996
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