EYS Is a Protein Associated with the Ciliary Axoneme in Rods and Cones

PURPOSE: Mutations in the EYS gene are a common cause of autosomal recessive retinitis pigmentosa (arRP), yet the role of the EYS protein in humans is presently unclear. The aim of this study was to investigate the isoform structure, expression and potential function of EYS in the mammalian retina i...

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Detalles Bibliográficos
Autores principales: Alfano, Giovanna, Kruczek, Przemyslaw M., Shah, Amna Z., Kramarz, Barbara, Jeffery, Glen, Zelhof, Andrew C., Bhattacharya, Shomi S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112921/
https://www.ncbi.nlm.nih.gov/pubmed/27846257
http://dx.doi.org/10.1371/journal.pone.0166397

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112921/
https://www.ncbi.nlm.nih.gov/pubmed/27846257
http://dx.doi.org/10.1371/journal.pone.0166397

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