IDENTIFIKASI MUTASI GEN β GLOBIN EKSON 1 PADA PEMBAWA THALASSEMIA

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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Bibliographic Details
Main Authors: , ANDIKA TRIPRAMUDYA ONGGO, , Dr. Niken Satuti Nur Handayani, M.Sc.
Format: Theses and Dissertations NonPeerReviewed
Published: [Yogyakarta] : Universitas Gadjah Mada 2014
Subjects:
ETD
Online Access:https://repository.ugm.ac.id/133119/
http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=73674
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Institution: Universitas Gadjah Mada

Internet

https://repository.ugm.ac.id/133119/
http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=73674

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