Article

Novel photobiomodulation therapy enhances color discrimination of color vision deficiency due to OPN1LW and/or OPN1MW gene mutations

2023-01-04

Abstract excerpt

<h4>Purpose</h4> To investigate the correlations of OPN1LW/OPN1MW (LW/MW) genotypes and clinical phenotypes in individuals with protan/deutan congenital color vision deficiency(CVD), and to explore photobiomodulation (PBM) therapy effects for CVD. <h4>Design</h4> Single-center consecutive, retrospective, observational study <h4>Participants</h4> 43 subjects (41 males and 2 females) of protan/deutan CVD from the se...

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Literature Corpus work: 1097e929-4d1e-5c8d-88ea-1616b4811ff3
DOI: 10.1101/2023.01.02.22284019

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