| License: Creative Commons Attribution 4.0 (2MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-404518
- DOI to cite this document:
- 10.5283/epub.40451
Abstract
X-linked juvenile retinoschisis (XLRS) is a hereditary retinal dystrophy, caused by mutations in the RS1 gene which encodes the secreted protein retinoschisin. In recent years, several molecules have been proposed to interact with retinoschisin, including the retinal Na/K-ATPase, L-voltage gated Ca2+ channels, and specific sugars. We recently showed that the retinal Na/K-ATPase consisting of ...

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