Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency

PURPOSE: Mutations in the coding sequence of the L and M opsin genes are often associated with X-linked cone dysfunction (such as Bornholm Eye Disease, BED), though the exact color vision phenotype associated with these disorders is variable. We examined individuals with L/M opsin gene mutations to...

Descripción completa

Detalles Bibliográficos
Autores principales: Patterson, Emily J., Wilk, Melissa, Langlo, Christopher S., Kasilian, Melissa, Ring, Michael, Hufnagel, Robert B., Dubis, Adam M., Tee, James J., Kalitzeos, Angelos, Gardner, Jessica C., Ahmed, Zubair M., Sisk, Robert A., Larsen, Michael, Sjoberg, Stacy, Connor, Thomas B., Dubra, Alfredo, Neitz, Jay, Hardcastle, Alison J., Neitz, Maureen, Michaelides, Michel, Carroll, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2016
Materias:
Visual Psychophysics and Physiological Optics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968428/
https://www.ncbi.nlm.nih.gov/pubmed/27447086
http://dx.doi.org/10.1167/iovs.16-19608

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968428/
https://www.ncbi.nlm.nih.gov/pubmed/27447086
http://dx.doi.org/10.1167/iovs.16-19608

Ejemplares similares