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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Association for Research in Vision and Ophthalmology
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017313/ https://www.ncbi.nlm.nih.gov/pubmed/27622081 http://dx.doi.org/10.1167/tvst.5.5.2 |