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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Опубликовано в: :Sci Rep
Главные авторы: 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.
Формат: Artigo
Язык:Inglês
Опубликовано: Nature Publishing Group UK 2017
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5593892/
https://ncbi.nlm.nih.gov/pubmed/28894305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-11679-y
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