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Identification of the retinoschisin-binding site on the retinal Na/K-ATPase

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 Ca(...

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Detalles Bibliográficos
Autores principales:	Plössl, Karolina, Straub, Kristina, Schmid, Verena, Strunz, Franziska, Wild, Jens, Merkl, Rainer, Weber, Bernhard H. F., Friedrich, Ulrike
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2019
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497308/ https://www.ncbi.nlm.nih.gov/pubmed/31048931 http://dx.doi.org/10.1371/journal.pone.0216320

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