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|Title: ||The spectrum of β-thalassemia mutations in Gaza Strip, Palestine|
|Authors: ||Sirdah, Mahmoud M|
Al-Yazji, Mansour S.
Tarazi d, Issa S.
Al-Haddad, Ramy M
Horstmann, Rolf D
|Issue Date: ||Apr-2013|
|Publisher: ||Blood Cells, Molecules, and Diseases|
|Citation: ||Volume 50, Issue 4, April 2013, Pages 247–251|
|Abstract: ||Background: β-Thalassemia is a disorder caused by mutations at the hemoglobin β-gene (HBB) locus.Its most important manifestation, the major form, is characterized by severe hypochromic and hemolytic anemia and is inherited in an autosomal recessive mode. In Gaza Strip, Palestine 0.02o/o of the population has been identified as B-thalassemia major.|
|Description: ||Article published in Blood Cells, Molecules, and Diseases. Volume 50, Issue 4, April 2013, Pages 247–251doi. Also available at www.elsevier.com/locate/bcmd|
|Appears in Collections:||Publications|
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