Gene therapy and gene-editing approaches to treat vision loss in a murine model of Acadian Usher syndrome

Authors

Katelyn N. Robillard, LSUHSC New OrleansFollow
Bhagwat V. Alapure, LSUHSC New OrleansFollow
Sanford L. Boye, University of Florida
Shannon E. Boye, University of Florida
Nicolas G. Bazan, LSUHSC New OrleansFollow
Jennifer J. Lentz, LSUHSC New OrleansFollow

Document Type

Article

Publication Date

6-1-2021

Publication Title

Investigative ophthalmology & visual science

Volume

62(8)

Comments

ARVO 2021

Recommended Citation

Robillard, Katelyn N.; Alapure, Bhagwat V.; Boye, Sanford L.; Boye, Shannon E.; Bazan, Nicolas G.; and Lentz, Jennifer J., "Gene therapy and gene-editing approaches to treat vision loss in a murine model of Acadian Usher syndrome" (2021). School of Medicine Faculty Publications. 1105.
https://digitalscholar.lsuhsc.edu/som_facpubs/1105