Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy-Reference-Cited by-同舟云学术

Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy

Published:2020-10 Issue: Volume:218 Page:40-53
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Oh Jin Kyun^ORCID,Ryu Joseph^ORCID,Lima de Carvalho Jose Ronaldo,Levi Sarah R.,Lee Winston,Tsamis Emmanouil^ORCID,Greenstein Vivienne C.,Mahajan Vinit B.^ORCID,Allikmets Rando,Tsang Stephen H.^ORCID

Funder

National Cancer Institute

National Eye Institute

National Institutes of Health

National Institute on Aging

Schneeweiss Stem Cell

Foundation Fighting Blindness

Research to Prevent Blindness

Publisher

Elsevier BV

Subject

Ophthalmology

Reference56 articles.

1. Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatism;Barthelmes;Invest Ophthalmol Vis Sci,2006

2. Foveal cavitation as an optical coherence tomography finding in central cone dysfunction;Leng;Retina,2012

3. Structural and genetic assessment of the ABCA4-associated optical gap phenotype;Nõupuu;Invest Ophthalmol Vis Sci,2014

4. Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsia;Greenberg;JAMA Ophthalmol,2014

5. Retinal development in infants and young children with achromatopsia;Lee;Ophthalmology,2015

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