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Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/M Opsin Interchange Mutations

PURPOSE: Human long (L) and middle (M) wavelength cone opsin genes are highly variable due to intermixing. Two L/M cone opsin interchange mutants, designated LIAVA and LVAVA, are associated with clinical diagnoses, including red-green color vision deficiency, blue cone monochromacy, cone degeneratio...

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Detalhes bibliográficos
Publicado no:Transl Vis Sci Technol
Main Authors: Greenwald, Scott H., Kuchenbecker, James A., Rowlan, Jessica S., Neitz, Jay, Neitz, Maureen
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5433808/
https://ncbi.nlm.nih.gov/pubmed/28516000
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/tvst.6.3.2
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