Beta thalassemia major: This form causes severe anemia, which can lead to potentially life-threatening complications without treatment. If you inherit a mutation of the HBB gene from one parent ...

Researchers have found a promising new method for gene therapy. They successfully restarted inactive genes by bringing them ...

Repositioning genes awakens fetal hemoglobin to treat disease. CRISPR editing may change future gene therapy. Researchers ...

The average Wall Street analyst following Editas Medicine ( EDIT 7.08%) thinks the gene therapy stock can reach $3.25 per ...

Although sickle cell disease (SCD) is not as widespread in the Philippines compared to other populations, it is still worth ...

A new study highlights a historic step in personalized medicine, utilizing CRISPR gene-editing technology for a ...

Learn about sickle cell disease, a genetic blood disorder affecting millions in India, with potential treatments and ...