License: Creative Commons Attribution 4.0 PDF - Published Version (6MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-527017
- DOI to cite this document:
- 10.5283/epub.52701
This publication is part of the DEAL contract with Springer.
Abstract
The RS1 gene on Xp 22.13 encodes retinoschisin which is known to directly interact with the retinal Na/K-ATPase at the photoreceptor inner segments. Pathologic mutations in RS1 cause X-linked juvenile retinoschisis (XLRS), a hereditary retinal dystrophy in young males. To further delineate the retinoschisin-Na/K-ATPase complex, co-immunoprecipitation was performed with porcine and murine retinal ...
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