Repair of a splicing defect in erythroid cells from patients with β-thalassemia/HbE disorder

A HeLa cell line stably expressing the human β-globin gene carrying thalassemic mutations βE/IVS1-6 served as a thalassemia model for repair of aberrant splicing of ΒE/IVS1-globin pre-mRNA with antisense oligonucleotides. Treatment of βE/IVS1-6 HeLa cells with a morpholino oligonucleotide targeted i...

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Bibliographic Details
Main Authors: Thipparat Suwanmanee, Halina Sierakowska, Suthat Fucharoen, Ryszard Kole
Other Authors: The University of North Carolina at Chapel Hill
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/20024
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Institution: Mahidol University

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