sgugenetics / -Sickle Cell Disease-
Single nucleotide polymorphisms (SNPs) in causing β-thalassemia
Supramolecular nanosubstrate–mediated delivery system enables CRISPR-Cas9 knockin of hemoglobin beta gene for hemoglobinopathies | Science Advances
File:HBB location.png - Wikipedia
Beta Thalassemia Causes | Understand Genetics & Inheritance
Identification of seven novel variants in the β-globin gene in transfusion-dependent and normal patients
What Causes Sickle Cell Disease?
What Causes Sickle Cell Disease?
Hemoglobin Disorders
Beta-thalassemia | Genetics in Medicine
Figure 1 from HBB FSC 36-37 (-T) Gene Mutation Detection in Carriers of Thalassemia Minor Using High Resolution Melting Analysis | Semantic Scholar
Map of human β-globin (HBB) gene and common indicated mutations along... | Download Scientific Diagram
Expression of β-globin by cancer cells promotes cell survival during blood-borne dissemination | Nature Communications
HBB-like gene cluster on chromosome 11 in sickle cell aremia. (A)... | Download Scientific Diagram
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
In Vivo Outcome of Homology-Directed Repair at the HBB Gene in HSC Using Alternative Donor Template Delivery Methods: Molecular Therapy - Nucleic Acids
Genetic Cause - Sickle Cell Disease
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
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
Frontiers | Regulatory Variation in Functionally Polymorphic Globin Genes of the Bank Vole: A Possible Role for Adaptation
Development of Gene Editing Strategies for Human β-Globin (HBB) Gene Mutations | bioRxiv
Sickle Cell Anemia: Genetics and Carrier Information - 23andMe
