Females heterozygous for congenital colour vision defects are of interest because they are believed to have cone photoreceptor ratios and cone photopigments that differ from normal. We describe a molecular genetic method to identify protan carriers that involves characterizing the genes that occur in the most upstream position in each of the X-chromosome photopigment gen
Mutations in the OPN1LW (L-) and OPN1MW (M-)cone opsin genes underlie a spectrum of cone photorecept...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
AbstractFemales heterozygous for congenital colour vision defects are of interest because they are b...
AbstractFemales heterozygous for congenital colour vision defects are of interest because they are b...
AbstractWe screened 150 male eye donors and identified four who did not have or express L pigment ge...
AbstractTwo sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as nor...
AbstractWe screened 150 male eye donors and identified four who did not have or express L pigment ge...
Inherited retinal degenerations are the leading cause of blindness in the working population. X-link...
AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild...
Thesis (Ph.D.)--University of Washington, 2015The long wavelength sensitive (L) and middle wavelengt...
Hereditary retinal disease is a significant cause of visual loss throughout the world. The underlyin...
X-linked progressive cone dystrophy (XLPCD) is characterized by progressive macular atrophy, abnorma...
PURPOSE: To perform a detailed clinical, psychophysical, and molecular assessment of members of 4 fa...
Colour vision is one of the visual functions which is very important in daily life. The phenomenon o...
Mutations in the OPN1LW (L-) and OPN1MW (M-)cone opsin genes underlie a spectrum of cone photorecept...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
AbstractFemales heterozygous for congenital colour vision defects are of interest because they are b...
AbstractFemales heterozygous for congenital colour vision defects are of interest because they are b...
AbstractWe screened 150 male eye donors and identified four who did not have or express L pigment ge...
AbstractTwo sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as nor...
AbstractWe screened 150 male eye donors and identified four who did not have or express L pigment ge...
Inherited retinal degenerations are the leading cause of blindness in the working population. X-link...
AbstractCarriers of X-linked color vision deficiencies have previously been reported to exhibit mild...
Thesis (Ph.D.)--University of Washington, 2015The long wavelength sensitive (L) and middle wavelengt...
Hereditary retinal disease is a significant cause of visual loss throughout the world. The underlyin...
X-linked progressive cone dystrophy (XLPCD) is characterized by progressive macular atrophy, abnorma...
PURPOSE: To perform a detailed clinical, psychophysical, and molecular assessment of members of 4 fa...
Colour vision is one of the visual functions which is very important in daily life. The phenomenon o...
Mutations in the OPN1LW (L-) and OPN1MW (M-)cone opsin genes underlie a spectrum of cone photorecept...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
We studied the scientific literature and disease guidelines in order to summarize the clinical utili...
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