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Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies
PURPOSE: The genetics underlying inherited color vision deficiencies is well understood: causative mutations change the copy number or sequence of the long (L), middle (M), or short (S) wavelength sensitive cone opsin genes. This study evaluated the potential of opsin gene analyses for use in clinic...
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| Publicado no: | Transl Vis Sci Technol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Association for Research in Vision and Ophthalmology
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5017313/ https://ncbi.nlm.nih.gov/pubmed/27622081 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/tvst.5.5.2 |
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