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Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East - ScienceDirect
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A Universal Approach to Correct Various HBB Gene Mutations in Human Stem Cells for Gene Therapy of Beta‐Thalassemia and Sickle Cell Disease - Cai - 2018 - STEM CELLS Translational Medicine - Wiley Online Library
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Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients
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Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study - ScienceDirect
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Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam | SpringerLink
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Figure 1 from HBB FSC 36-37 (-T) Gene Mutation Detection in Carriers of Thalassemia Minor Using High Resolution Melting Analysis | Semantic Scholar
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Upper panel, schematic presentation of the HBB gene and the relative... | Download Scientific Diagram
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CRISPR/Cas9 mediated genome editing of the human HBB gene by its cDNA.... | Download Scientific Diagram
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Supramolecular nanosubstrate–mediated delivery system enables CRISPR-Cas9 knockin of hemoglobin beta gene for hemoglobinopathies | Science Advances
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In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods: Molecular Therapy - Nucleic Acids
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