Sickle Cell Genetics
2: Sickle Cell Disease — Dr Julia Morris
Upper panel, schematic presentation of the HBB gene and the relative... | Download Scientific Diagram
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
HBB gene structure denoting both the studied mutation. | Download Scientific Diagram
Beta-thalassemia | Genetics in Medicine
Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients
Beta Thalassemia Causes | Understand Genetics & Inheritance
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
Development of Gene Editing Strategies for Human β-Globin (HBB) Gene Mutations | bioRxiv
Hemoglobin Disorders
Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam | SpringerLink
Sickle Cell Genetics
Figure 1 from HBB FSC 36-37 (-T) Gene Mutation Detection in Carriers of Thalassemia Minor Using High Resolution Melting Analysis | Semantic Scholar
HBB Gene - GeneCards | HBB Protein | HBB Antibody
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
Single nucleotide polymorphisms (SNPs) in causing β-thalassemia
In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods: Molecular Therapy - Nucleic Acids
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
Development of gene editing strategies for human β-globin (HBB) gene mutations - ScienceDirect
HBB Gene - GeneCards | HBB Protein | HBB Antibody
Hemoglobin Disorders
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
