Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure

Deleterious mutations in RS1 encoding retinoschisin are associated with X-linked juvenile retinoschisis (RS), a common form of macular degeneration in males. The disorder is characterized by a negative electroretinogram pattern and by a splitting of the inner retina. To gain further insight into the...

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Detalles Bibliográficos
Main Authors: Weber, Bernhard H. F., Schrewe, Heinrich, Molday, Laurie L., Gehrig, Andrea, White, Karen L., Seeliger, Mathias W., Jaissle, Gesine B., Friedburg, Christoph, Tamm, Ernst, Molday, Robert S.
Formato: Artigo
Idioma:Inglês
Publicado: The National Academy of Sciences 2002
Assuntos:
Biological Sciences
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC122930/
https://ncbi.nlm.nih.gov/pubmed/11983912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.092528599
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