Development of gene editing strategies for human β-globin (HBB) gene mutations - ScienceDirect
Sickle Cell Genetics
Hemoglobin Disorders
Frontiers | Regulatory Variation in Functionally Polymorphic Globin Genes of the Bank Vole: A Possible Role for Adaptation
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
Supramolecular nanosubstrate–mediated delivery system enables CRISPR-Cas9 knockin of hemoglobin beta gene for hemoglobinopathies | Science Advances
HBB Gene - GeneCards | HBB Protein | HBB Antibody
Hemoglobin Disorders
Genetic Cause - Sickle Cell Disease
Sickle Cell Anemia: Genetics and Carrier Information - 23andMe
Expression of β-globin by cancer cells promotes cell survival during blood-borne dissemination | Nature Communications
In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods: Molecular Therapy - Nucleic Acids
2: Sickle Cell Disease — Dr Julia Morris
Hemoglobin Disorders
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
File:HBB location.png - Wikipedia
Single nucleotide polymorphisms (SNPs) in causing β-thalassemia
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
HBB gene structure denoting both the studied mutation. | Download Scientific Diagram
Upper panel, schematic presentation of the HBB gene and the relative... | Download Scientific Diagram
Hemoglobin subunit beta - Wikipedia
Beta Thalassemia Causes | Understand Genetics & Inheritance
