Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients

Usher syndrome is an inherited and irreversible disease that manifests as retinitis pigmentosa (RP) and bilateral neurosensory hearing loss. Mutations in Usherin 2A (USH2A) are not only a frequent cause of Usher syndrome, but also nonsyndromic RP. Although gene- and cell-based therapies are on the h...

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Detalles Bibliográficos
Autores principales: Sengillo, Jesse D., Cabral, Thiago, Schuerch, Kaspar, Duong, Jimmy, Lee, Winston, Boudreault, Katherine, Xu, Yu, Justus, Sally, Sparrow, Janet R., Mahajan, Vinit B., Tsang, Stephen H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593892/
https://www.ncbi.nlm.nih.gov/pubmed/28894305
http://dx.doi.org/10.1038/s41598-017-11679-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593892/
https://www.ncbi.nlm.nih.gov/pubmed/28894305
http://dx.doi.org/10.1038/s41598-017-11679-y

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