Gene's hubs in retinal diseases: A retinal disease network

BACKGROUND: Retinal diseases associated with the dysfunction or death of photoreceptors are a major cause of blindness around the world, improvements in genetics tools, like next generation sequencing (NGS) allows the discovery of genes and genetic changes that lead to many of those retinal diseases...

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Detalles Bibliográficos
Autores principales: Lázaro-Guevara, J.M., Flores-Robles, B.J., Garrido, K., Pinillos-Aransay, V., Elena-Ibáñez, A., Merino-Meléndez, L., López-Martínez, J.A., Victoriano-Lacalle, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218668/
https://www.ncbi.nlm.nih.gov/pubmed/30417144
http://dx.doi.org/10.1016/j.heliyon.2018.e00867

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218668/
https://www.ncbi.nlm.nih.gov/pubmed/30417144
http://dx.doi.org/10.1016/j.heliyon.2018.e00867

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