Genomic approaches to identifying targets for treating β hemoglobinopathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/article/10.1186/s12920-015-0120-2/fulltext.html
Reference148 articles.
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2. Piel FB, Weatherall DJ. The alpha-thalassemias. N Engl J Med. 2014;371:1908–16.
3. Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anaemia in children under five, 2010–2050: modelling based on demographics, excess mortality, and interventions. PLoS Med. 2013;10:e1001484.
4. Colah R, Gorakshakar A, Nadkarni A. Global burden, distribution and prevention of beta-thalassemias and hemoglobin E disorders. Expert Rev Hematol. 2010;3:103–17.
5. Organization WH. Management of Haemoglobin Disorders, Report of Joint WHO/TIF Meeting. Nicosia: Cyprus; 2007.
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