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...

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محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:Invest Ophthalmol Vis Sci
المؤلفون الرئيسيون: 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
التنسيق: Artigo
اللغة:Inglês
منشور في: The Association for Research in Vision and Ophthalmology 2016
الموضوعات:
Visual Psychophysics and Physiological Optics
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC4968428/
https://ncbi.nlm.nih.gov/pubmed/27447086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.16-19608
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