QuickView for USH2A;jsessionid=2C182DA29728D929DD6A8F6D02517B76;jsessionid=0924B9D2C463EDB33194C5311B041346;jsessionid=47AF04D5048A89C97BBB427AE3E20B28;jsessionid=FE6EEECFC02F38E902AC739E71365D0F (gene)

1. USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort …
2. Generation of the induced pluripotent stem cell line SFMUi001-A from a patient with usher syndrome t…
3. Successful large gene augmentation of USH2A with non-viral episomal vectors.
4. USH2A Gene Mutations in Rabbits Lead to Progressive Retinal Degeneration and Hearing Loss.
5. Exome sequencing identified five novel USH2A variants in Korean patients with retinitis pigmentosa.

There were no clinical trials for USH2A;jsessionid=2C182DA29728D929DD6A8F6D02517B76;jsessionid=0924B9D2C463EDB33194C5311B041346;jsessionid=47AF04D5048A89C97BBB427AE3E20B28;jsessionid=FE6EEECFC02F38E902AC739E71365D0F