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http://hdl.handle.net/123456789/6726
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| Title: | The spectrum of β-thalassemia mutations in Gaza Strip, Palestine |
| Authors: | Sirdah, Mahmoud M
Sievertsen, Jürgen
Al-Yazji, Mansour S.
Tarazi d, Issa S.
Al-Haddad, Ramy M
Horstmann, Rolf D
Timmann, Christian |
| Keywords: | Hemoglobin
Beta thalassemia
DASH
Hybridization
Sequencing |
| 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 |
| URI: | http://hdl.handle.net/123456789/6726 |
| Appears in Collections: | Publications
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