Dissecting the role of EYS in retinal degeneration: clinical and molecular aspects and its implications for future therapy

Mutations in the EYS gene are one of the major causes of autosomal recessive retinitis pigmentosa. EYS-retinopathy presents a severe clinical phenotype, and patients currently have no therapeutic options. The progress in personalised medicine and gene and cell therapies hold promise for treating thi...

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Detalles Bibliográficos
Autores principales: Garcia-Delgado, Ana B., Valdes-Sanchez, Lourdes, Morillo-Sanchez, Maria Jose, Ponte-Zuñiga, Beatriz, Diaz-Corrales, Francisco J., de la Cerda, Berta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127272/
https://www.ncbi.nlm.nih.gov/pubmed/34001227
http://dx.doi.org/10.1186/s13023-021-01843-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127272/
https://www.ncbi.nlm.nih.gov/pubmed/34001227
http://dx.doi.org/10.1186/s13023-021-01843-z

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