MOLECULAR VARIANTS OF BETA-THALASSEMIA IN EGYPT

Nagham Youssef Mohammed;

Abstract


-thalassemia is one of the genetic diseases which can be broadly defined as a syndrome of inherited hemoglobin disorders characterized by a quantitative deficiency of functional -globin chains.
Beta thalassemia is caused by any of more than 200 mutatio


Other data

Title MOLECULAR VARIANTS OF BETA-THALASSEMIA IN EGYPT
Other Titles الأنماط الجزيئية لانيميا البحر المتوسط (ب) فى مصر
Authors Nagham Youssef Mohammed
Keywords MOLECULAR VARIANTS OF BETA-THALASSEMIA IN EGYPT
Issue Date 2009
Description 
-thalassemia is one of the genetic diseases which can be broadly defined as a syndrome of inherited hemoglobin disorders characterized by a quantitative deficiency of functional -globin chains.
Beta thalassemia is caused by any of more than 200 mutatio

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