HIGH PREVALENCE OF RARE MUTATIONS IN THE BETA GLOBIN GENE IN AN ETHNIC GROUP IN IRAN (LETTER TO THE EDITOR)

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GALEHDARI H.; SALEHI B.; PEDRAM M.; ORAKI KOHSHOUR M.

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Journal Paper

Paper Information

Journal: Iranian Red Crescent Medical Journal Year:2011 | Volume:13 | Issue:5 Page(s): 356-358

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Title

HIGH PREVALENCE OF RARE MUTATIONS IN THE BETA GLOBIN GENE IN AN ETHNIC GROUP IN IRAN (LETTER TO THE EDITOR)

Author(s)

GALEHDARI H. | SALEHI B. | PEDRAM M. | ORAKI KOHSHOUR M. | Issue Writer Certificate

Keywords

BETA THALASSEMIA

EIZEH

BAQ-MALEK

IRAN

BAKHTIARI

MUTATIONS

Abstract

BETA THALASSEMIA major is a genetic disease with an autosomal recessive pattern and is differentiated by severe microcytic hypochromic hemolytic anemia with hepatosplenomegaly, ineffective erythropoiesis and bone marrow expansion.1 The b-globin (HBB) gene coding for b-chain expression is located on a 50 kb globin gene cluster on the short arm of chromosome 11, whose mutation mediated inactivation is usually responsive for the outcome of disease. BETA THALASSEMIA occurs frequently in the coastline areas of the world.

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APA: Copy

GALEHDARI, H., SALEHI, B., PEDRAM, M., & ORAKI KOHSHOUR, M.. (2011). HIGH PREVALENCE OF RARE MUTATIONS IN THE BETA GLOBIN GENE IN AN ETHNIC GROUP IN IRAN (LETTER TO THE EDITOR). IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ), 13(5), 356-358. SID. https://sid.ir/paper/292381/en

Vancouver: Copy

GALEHDARI H., SALEHI B., PEDRAM M., ORAKI KOHSHOUR M.. HIGH PREVALENCE OF RARE MUTATIONS IN THE BETA GLOBIN GENE IN AN ETHNIC GROUP IN IRAN (LETTER TO THE EDITOR). IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ)[Internet]. 2011;13(5):356-358. Available from: https://sid.ir/paper/292381/en

IEEE: Copy

H. GALEHDARI, B. SALEHI, M. PEDRAM, and M. ORAKI KOHSHOUR, “HIGH PREVALENCE OF RARE MUTATIONS IN THE BETA GLOBIN GENE IN AN ETHNIC GROUP IN IRAN (LETTER TO THE EDITOR),” IRANIAN RED CRESCENT MEDICAL JOURNAL (IRCMJ), vol. 13, no. 5, pp. 356–358, 2011, [Online]. Available: https://sid.ir/paper/292381/en

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