Photoreceptor-Specific Temporal Contrast Sensitivities in RP1L1-Associated Occult Macular Dystrophy

Author:

Huchzermeyer Cord1,Fars Julien1,Kremers Jan1,Kühlewein Laura2,Kempf Melanie2,Ott Saskia2,Stingl Krunoslav2,Stingl Katarina2

Affiliation:

1. Department of Ophthalmology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany

2. Center for Ophthalmology, University Hospital Tübingen, Tübingen, Germany

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

Reference51 articles.

1. Phenotype variations caused by mutations in the RP1L1 gene in a large mainly German cohort;Zobor;Invest Ophthalmol Vis Sci,2018

2. New techniques for quantification of color vision in disorders of cone function?: Cambridge color test and photoreceptor-specific temporal contrast sensitivity in patients with heterozygous RP1L1 and RPGR mutations];Huchzermeyer;Ophthalmol Z Dtsch Ophthalmol Ges,2021

3. Visual field characteristics in East Asian patients with occult macular dystrophy (Miyake disease): EAOMD report no. 3;Ahn;Invest Ophthalmol Vis Sci,2022

4. Clinical stages of occult macular dystrophy based on optical coherence tomographic findings;Nakamura;Invest Ophthalmol Vis Sci,2019

5. Characterizing the phenotype and genotype of a family with occult macular dystrophy;Chen;Arch Ophthalmol Chic Ill 1960,2012

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