Toward a Therapy for a Rare Genetic Disease
HMS News article on new research from David Corey, Artur A Indzhykulian, and colleagues, first author Maryna Ivanchenko. Using mice, the team designed a “mini gene” that could in the future be developed into a therapy for Usher Syndrome type 1F, a severe genetic condition that causes blindness and deafness.
News Types: In the News