Discovery of genetic glitches in gene formatting (RNU4-2 mutations) discloses a new cause for blindness, solving retinal ...

About the LUCE-1 Trial LUCE-1 is a Phase 1/2 multicenter, open-label, dose escalation study investigating safety, tolerability and preliminary efficacy of 3 dose levels of dual AAV8.MYO7A (AAVB-081) ...

Researchers led by the Institute of Molecular and Clinical Ophthalmology Basel uncovered disease-causing variants in ...

Diagnosed with retinitis pigmentosa, Anne Hatton Ogden uses cooking as a form of therapy. With guide dog Angelo and assistive ...

IOB researchers, in collaboration with a team from Radboud University Medical Center and partners from more than 100 institutions worldwide, identify new genetic cause of inherited blindness. The ...

A blind sailor is aiming for the Paralympics in Brisbane in 2032, after winning medals in the World Sailing Inclusion ...

Researchers from Radboud University Medical Center and University of Basel have discovered new genetic causes of inherited ...

In patients with retinitis pigmentosa (RP), crucial cells in the retina known as rods and cones die over time; night ...

A special art show at Bryn Mawr Rehab Hospital aims to raise community awareness about cognitive and physical disabilities.

People should do these checks often, whether they are just starting to drive or have been behind the wheel for years ...

Parents and students at the Arizona State Schools for the Deaf and Blind (ASDB) Tucson campus continue to speak out against ...