Explore how CRISPR gene editing is transforming the treatment of inherited blindness through groundbreaking clinical trials and innovative therapies.
Explore how CRISPR-Cas9 is transforming hematology, from curing sickle cell disease to personalized gene therapies for rare blood disorders.
How CRISPR/Cas9 gene-editing technology offers hope for curing Duchenne Muscular Dystrophy by correcting the root genetic cause of this devastating disorder.
Exploring the revolutionary technologies transforming ophthalmology in 2025 - from AI diagnostics to gene therapy and smart wearables.