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OPN1LW gene

Known as: OPN1LW, RED CONE PIGMENT, OPSIN 1, LONG-WAVE-SENSITIVE 
National Institutes of Health

Related topics

Related topics

2 relations
Color Blindness, RedOPN1MW gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
Purpose To present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene… 
2017
2017
Evolutionary analysis of vision genes identifies potential drivers of visual differences between giraffe and okapi
Background The capacity of visually oriented species to perceive and respond to visual signal is integral to their evolutionary… 
2016
2016
Visual Psychophysics and Physiological Optics Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency
Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin, United States Cell Biology, Neurobiology and… 
2015
2015
Confirmation of variants in OPN1LW as a common cause of MYP1 based on study of Chinese families with nonsyndromic high myopia
2013
2013
Exon 3 genotypes of OPN1LW/OPN1MW associated with X-linked congenital cone dysfunction
2011
2011
Mutation Analysis Of The OPN1LW And OPN1MW Cone Opsin Genes In A Cohort Of British Families With Blue Cone Monochromacy
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