Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam | SpringerLink
Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study - ScienceDirect
Supramolecular nanosubstrate–mediated delivery system enables CRISPR-Cas9 knockin of hemoglobin beta gene for hemoglobinopathies | Science Advances
Hemoglobin subunit beta - Wikipedia
Map of human β-globin (HBB) gene and common indicated mutations along... | Download Scientific Diagram
Single nucleotide polymorphisms (SNPs) in causing β-thalassemia
Sickle Cell Genetics
Hemoglobin Disorders
Hemoglobin Disorders
In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods: Molecular Therapy - Nucleic Acids
Genes | Free Full-Text | Spatial and Temporal Expression Characteristics of the HBB Gene Family in Six Different Pig Breeds
Hemoglobin Disorders
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
David R. Liu on Twitter: "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
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
Frontiers | Regulatory Variation in Functionally Polymorphic Globin Genes of the Bank Vole: A Possible Role for Adaptation
sgugenetics / -Sickle Cell Disease-
What Causes Sickle Cell Disease?
Development of Gene Editing Strategies for Human β-Globin (HBB) Gene Mutations | bioRxiv
Does size matter? Two new deletions in the HBB gene cause β0-thalassemia | SpringerLink
HBB Gene Structure - Human Hemoglobin (HbA) and the HBB gene
HBB gene structure denoting both the studied mutation. | Download Scientific Diagram
What Causes Sickle Cell Disease?
Beta-thalassemia | Genetics in Medicine
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
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
Development of gene editing strategies for human β-globin (HBB) gene mutations - ScienceDirect
