Widening the spectrum of deletions and molecular mechanisms underlying alpha-thalassemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/article/10.1007/s00277-017-3090-y/fulltext.html
Reference30 articles.
1. Higgs DR (2013) The molecular basis of α-thalassemia. Cold Spring Harb Perspect Med 3(1):a011718. doi: 10.1101/cshperspect.a011718
2. Hatton CS, Wilkie AO, Drysdale HC, Wood WG, Vickers MA, Sharpe J, Ayyub H, Pretorius IM, Buckle VJ, Higgs DR (1990) Alpha-thalassemia caused by a large (62kb) deletion upstream of the human alpha globin gene cluster. Blood 76(1):221–227
3. Romão L, Osorio-Almeida L, Higgs DR, Lavinha J, Liebhaber SA (1991) α-Thalassemia resulting from deletion of regulatory sequences far upstream of the α-globin structural gene. Blood 78(6):1589–1595
4. Viprakasit V, Kidd AM, Ayyub H, Horsley S, Hughes J, Higgs DR (2003) De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia. Br J Haematol 120(5):867–875. doi: 10.1046/j.1365-2141.2003.04197.x
5. Viprakasit V, Harteveld CL, Ayyub H, Stanley JS, Giordano PC, Wood WG, Higgs DR (2006) A novel deletion causing α-thalassemia clarifies the importance of the major human alpha globin regulatory element. Blood 107(9):3811–3812. doi: 10.1182/blood-2005-12-4834
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