IDENTIFIKASI MUTASI GEN β GLOBIN EKSON 1 PADA PEMBAWA THALASSEMIA
Thalassemia is an autosomal recessive genetic mutation disorder with symptoms similliar to anemia that causes deficiency synthesis of the globin chains (hemoglobin component inside erythrocytes). Thalassemia is classified based on secondary protein structure abnormalities in α globin protein or β...
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| Format: | Thesis |
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[Yogyakarta] : Universitas Gadjah Mada
2014
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