Gene Therapy

CRISPR/Cas9-based gene editing holds immense promise for restoring auditory function in individuals with genetic hearing impairments. By precisely targeting and correcting disease-causing mutations, this technology offers a transformative approach to address the underlying genetic basis of hearing loss.

CRISPR/Cas9 technology offers a revolutionary approach to gene therapy for retinal diseases, addressing limitations such as off-target effects, immune responses, and delivery challenges. By providing precise gene editing and enhanced delivery methods, CRISPR/Cas9 holds promise for treating genetic disorders and restoring vision.