The Xmn1 polymorphic site 5′ to the Gγ gene and its correlation to the Gγ:Aγ ratio, age at first blood transfusion and clinical features in β-Thalassemia patients from Western Iran
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11033-009-9566-7.pdf
Reference34 articles.
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3. Rund D, Rachmilewitz E (2005) Beta-thalassemia. N Engl J Med 353:1135–1146. doi: 10.1056/NEJMra050436
4. Charache S, Terrin ML, Moore RD et al (1995) Effects of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the multicenter study of hydroxyurea in sickle cell anemia. N Engl J Med 332:1317–1322. doi: 10.1056/NEJM199505183322001
5. Zimmerman S, Schultz W, Davis J et al (2004) Sustained long-term hematological efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood 103:2039–2045. doi: 10.1182/blood-2003-07-2475
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