| PDF - Published Version (6MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-352116
- DOI to cite this document:
- 10.5283/epub.35211
Abstract
X-linked juvenile retinoschisis is a heritable condition of the retina in males caused by mutations in the RS1 gene. Still, the cellular function and retina-specific expression of RS1 are poorly understood. To address the latter issue, we characterized the minimal promoter driving expression of RS1 in the retina. Binding site prediction, site-directed mutagenesis, and reporter assays suggest an ...
Owner only: item control page