In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods: Molecular Therapy - Nucleic Acids
HBB gene structure denoting both the studied mutation. | Download Scientific Diagram
Genes | Free Full-Text | Spatial and Temporal Expression Characteristics of the HBB Gene Family in Six Different Pig Breeds
Hemoglobin Disorders
Figure 1 from Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study | Semantic Scholar
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
Frontiers | Regulatory Variation in Functionally Polymorphic Globin Genes of the Bank Vole: A Possible Role for Adaptation
Hemoglobin subunit beta - Wikipedia
Development of gene editing strategies for human β-globin (HBB) gene mutations - ScienceDirect
Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR) | BMC Medical Genetics
Sickle Cell Genetics
Map of human β-globin (HBB) gene and common indicated mutations along... | Download Scientific Diagram
Hemoglobin Disorders
Development of Gene Editing Strategies for Human β-Globin (HBB) Gene Mutations | bioRxiv
Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study - ScienceDirect
What Causes Sickle Cell Disease?
Does size matter? Two new deletions in the HBB gene cause β0-thalassemia | SpringerLink
File:HBB location.png - Wikipedia
Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients
Figure 1 from HBB FSC 36-37 (-T) Gene Mutation Detection in Carriers of Thalassemia Minor Using High Resolution Melting Analysis | Semantic Scholar
Genetic Cause - Sickle Cell Disease
Sickle Cell Anemia: Genetics and Carrier Information - 23andMe
HBB Gene - GeneCards | HBB Protein | HBB Antibody
David R. Liu on X: "Each year more than 300,000 are born with SCD—the result of inheriting 2 mutated copies of the HBB gene. The mutated hemoglobin polymerizes, causing sickle-shaped red blood
Hemoglobin Disorders
2: Sickle Cell Disease — Dr Julia Morris
