Genetic testing for color vision deficiency
نویسندگان
چکیده
منابع مشابه
acquired color vision deficiency in parkinson’s disease
acquired color deficiency in the tritan axis in parkinson’s disease has already been reported, manifesting itself as impaired performance in various visual tasks. however, its clinical significance has always been controversial. in this study we evaluated the performance of parkinson s disease patients in lanthony 15-desaturated clinical test and for the first time, compared it with the standar...
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We report a functional reflective polarizer that can be incorporated into a compact augmented reality system. The design principle of the functional reflective polarizer is explained and two design examples are illustrated. In the first example, with the specially designed functional reflective polarizer, the transmittance of the augment reality system is relatively high as compared to a polari...
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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 clinical diagnosis of color vision defects. METHODS We tested 1872 human subjects using direct sequenc...
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ژورنال
عنوان ژورنال: The EuroBiotech Journal
سال: 2017
ISSN: 2564-615X
DOI: 10.24190/issn2564-615x/2017/s1.10