Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments

Usher syndrome type 1 (USH1) is a major cause of inherited deafness and blindness in humans. The eye disorder is often referred to as retinitis pigmentosa, which is characterized by a secondary cone degeneration following the rod loss. The development of treatments to prevent retinal degeneration ha...

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Detalles Bibliográficos
Autores principales: Trouillet, Alix, Dubus, Elisabeth, Dégardin, Julie, Estivalet, Amrit, Ivkovic, Ivana, Godefroy, David, García-Ayuso, Diego, Simonutti, Manuel, Sahly, Iman, Sahel, José A., El-Amraoui, Aziz, Petit, Christine, Picaud, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792440/
https://www.ncbi.nlm.nih.gov/pubmed/29386551
http://dx.doi.org/10.1038/s41598-018-20171-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792440/
https://www.ncbi.nlm.nih.gov/pubmed/29386551
http://dx.doi.org/10.1038/s41598-018-20171-0

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