{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,12]],"date-time":"2026-05-12T00:42:46Z","timestamp":1778546566976,"version":"3.51.4"},"reference-count":56,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2020,10,1]],"date-time":"2020-10-01T00:00:00Z","timestamp":1601510400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,10,1]],"date-time":"2020-10-01T00:00:00Z","timestamp":1601510400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/100001116","name":"Foundation Fighting Blindness","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001116","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100001818","name":"Research to Prevent Blindness","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001818","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100001116","name":"Foundation Fighting Blindness","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001116","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["ajo.com","clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["American Journal of Ophthalmology"],"published-print":{"date-parts":[[2020,10]]},"DOI":"10.1016\/j.ajo.2020.05.016","type":"journal-article","created":{"date-parts":[[2020,5,20]],"date-time":"2020-05-20T21:13:07Z","timestamp":1590009187000},"page":"40-53","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":13,"special_numbering":"C","title":["Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy"],"prefix":"10.1016","volume":"218","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5350-9412","authenticated-orcid":false,"given":"Jin Kyun","family":"Oh","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5449-2395","authenticated-orcid":false,"given":"Joseph","family":"Ryu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"suffix":"Jr.","given":"Jose Ronaldo","family":"Lima de Carvalho","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sarah R.","family":"Levi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Winston","family":"Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7418-1033","authenticated-orcid":false,"given":"Emmanouil","family":"Tsamis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Vivienne C.","family":"Greenstein","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1886-1741","authenticated-orcid":false,"given":"Vinit B.","family":"Mahajan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rando","family":"Allikmets","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9082-2427","authenticated-orcid":false,"given":"Stephen H.","family":"Tsang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"3","key":"10.1016\/j.ajo.2020.05.016_bib1","doi-asserted-by":"crossref","first-page":"1161","DOI":"10.1167\/iovs.05-0783","article-title":"Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatism","volume":"47","author":"Barthelmes","year":"2006","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"7","key":"10.1016\/j.ajo.2020.05.016_bib2","doi-asserted-by":"crossref","first-page":"1411","DOI":"10.1097\/IAE.0b013e318236e4ea","article-title":"Foveal cavitation as an optical coherence tomography finding in central cone dysfunction","volume":"32","author":"Leng","year":"2012","journal-title":"Retina"},{"issue":"11","key":"10.1016\/j.ajo.2020.05.016_bib3","doi-asserted-by":"crossref","first-page":"7217","DOI":"10.1167\/iovs.14-14674","article-title":"Structural and genetic assessment of the ABCA4-associated optical gap phenotype","volume":"55","author":"N\u00f5upuu","year":"2014","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"4","key":"10.1016\/j.ajo.2020.05.016_bib4","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1001\/jamaophthalmol.2013.7987","article-title":"Spectral-domain optical coherence tomography staging and autofluorescence imaging in achromatopsia","volume":"132","author":"Greenberg","year":"2014","journal-title":"JAMA Ophthalmol"},{"issue":"10","key":"10.1016\/j.ajo.2020.05.016_bib5","doi-asserted-by":"crossref","first-page":"2145","DOI":"10.1016\/j.ophtha.2015.03.033","article-title":"Retinal development in infants and young children with achromatopsia","volume":"122","author":"Lee","year":"2015","journal-title":"Ophthalmology"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib6","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/s10633-014-9473-7","article-title":"ISCEV standard for full-field clinical electroretinography (2015 update)","volume":"130","author":"McCulloch","year":"2015","journal-title":"Doc Ophthalmol"},{"issue":"5","key":"10.1016\/j.ajo.2020.05.016_bib7","doi-asserted-by":"crossref","first-page":"2328","DOI":"10.1167\/iovs.08-2936","article-title":"Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography","volume":"50","author":"Hood","year":"2009","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"7","key":"10.1016\/j.ajo.2020.05.016_bib8","doi-asserted-by":"crossref","first-page":"757","DOI":"10.1038\/ng.3319","article-title":"Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia","volume":"47","author":"Kohl","year":"2015","journal-title":"Nat Genet"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib9","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1016\/j.ajhg.2013.05.005","article-title":"Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy","volume":"93","author":"Roosing","year":"2013","journal-title":"Am J Hum Genet"},{"issue":"3","key":"10.1016\/j.ajo.2020.05.016_bib10","doi-asserted-by":"crossref","first-page":"139","DOI":"10.3109\/13816810.2010.486776","article-title":"PITPNM3 is an uncommon cause of cone and cone-rod dystrophies","volume":"31","author":"K\u00f6hn","year":"2010","journal-title":"Ophthalmic Genet"},{"issue":"6","key":"10.1016\/j.ajo.2020.05.016_bib11","doi-asserted-by":"crossref","first-page":"664","DOI":"10.1038\/sj.ejhg.5201817","article-title":"Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families","volume":"15","author":"Kohn","year":"2007","journal-title":"Eur J Hum Genet"},{"issue":"1-2","key":"10.1016\/j.ajo.2020.05.016_bib12","doi-asserted-by":"crossref","first-page":"75","DOI":"10.3109\/13816810.2012.707271","article-title":"Abnormality in the external limiting membrane in early Stargardt disease","volume":"34","author":"Burke","year":"2013","journal-title":"Ophthalmic Genet"},{"issue":"5","key":"10.1016\/j.ajo.2020.05.016_bib13","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1016\/j.ophtha.2017.11.020","article-title":"Early patterns of macular degeneration in ABCA4-associated retinopathy","volume":"125","author":"Khan","year":"2018","journal-title":"Ophthalmology"},{"issue":"15","key":"10.1016\/j.ajo.2020.05.016_bib14","doi-asserted-by":"crossref","first-page":"5735","DOI":"10.1167\/iovs.18-25452","article-title":"Longitudinal assessment of retinal structure in achromatopsia patients with long-term follow-up","volume":"59","author":"Hirji","year":"2018","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib15","doi-asserted-by":"crossref","first-page":"19","DOI":"10.3341\/kjo.2013.27.1.19","article-title":"Morphologic characteristics of the outer retina in cone dystrophy on spectral-domain optical coherence tomography","volume":"27","author":"Cho","year":"2013","journal-title":"Korean J Ophthalmol"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib16","doi-asserted-by":"crossref","first-page":"56","DOI":"10.1097\/ICB.0b013e3181cd1d8b","article-title":"Use of spectral domain-optical coherence tomography to visualize photoreceptor abnormalities in cone-rod dystrophy 6","volume":"5","author":"Kim","year":"2011","journal-title":"Retin Cases Brief Rep"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib17","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1016\/j.exer.2009.02.001","article-title":"G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull\u2019s eye maculopathy","volume":"89","author":"Cella","year":"2009","journal-title":"Exp Eye Res"},{"key":"10.1016\/j.ajo.2020.05.016_bib18","series-title":"Heidelberg Engineering. Spectralis hardware operating instructions. Technical Specifications","first-page":"22","year":"2007"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib19","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1159\/000342159","article-title":"Hyperreflective dots: a new spectral-domain optical coherence tomography entity for follow-up and prognosis in exudative age-related macular degeneration","volume":"229","author":"Coscas","year":"2013","journal-title":"Ophthalmologica"},{"key":"10.1016\/j.ajo.2020.05.016_bib20","doi-asserted-by":"crossref","first-page":"e28899","DOI":"10.7554\/eLife.28899","article-title":"Biochemical adaptations of the retina and retinal pigment epithelium support a metabolic ecosystem in the vertebrate eye","volume":"6","author":"Kanow","year":"2017","journal-title":"Elife"},{"issue":"8","key":"10.1016\/j.ajo.2020.05.016_bib21","doi-asserted-by":"crossref","first-page":"2061","DOI":"10.1523\/JNEUROSCI.2689-16.2017","article-title":"Mitochondria maintain distinct Ca2+ pools in cone photoreceptors","volume":"37","author":"Giarmarco","year":"2017","journal-title":"J Neurosci"},{"issue":"11","key":"10.1016\/j.ajo.2020.05.016_bib22","doi-asserted-by":"crossref","first-page":"5952","DOI":"10.1167\/iovs.10-5680","article-title":"Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography","volume":"51","author":"Thiadens","year":"2010","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"6","key":"10.1016\/j.ajo.2020.05.016_bib23","doi-asserted-by":"crossref","first-page":"1211","DOI":"10.1016\/j.ajo.2013.06.033","article-title":"Diagnostic fundus autofluorescence patterns in achromatopsia","volume":"156","author":"Fahim","year":"2013","journal-title":"Am J Ophthalmol"},{"issue":"10","key":"10.1016\/j.ajo.2020.05.016_bib24","doi-asserted-by":"crossref","first-page":"7298","DOI":"10.1167\/iovs.11-7762","article-title":"Photoreceptor structure and function in patients with congenital achromatopsia","volume":"52","author":"Genead","year":"2011","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib25","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1016\/j.ophtha.2013.08.017","article-title":"Retinal structure and function in achromatopsia: implications for gene therapy","volume":"121","author":"Sundaram","year":"2014","journal-title":"Ophthalmology"},{"issue":"2","key":"10.1016\/j.ajo.2020.05.016_bib26","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1016\/j.ajhg.2009.06.016","article-title":"Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders","volume":"85","author":"Thiadens","year":"2009","journal-title":"Am J Hum Genet"},{"issue":"9","key":"10.1016\/j.ajo.2020.05.016_bib27","doi-asserted-by":"crossref","first-page":"1232","DOI":"10.1136\/bjophthalmol-2012-301737","article-title":"Early signs of longitudinal progressive cone photoreceptor degeneration in achromatopsia","volume":"96","author":"Thomas","year":"2012","journal-title":"Br J Ophthalmol"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib28","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1007\/s10384-016-0484-7","article-title":"In\u00a0vivo imaging of a cone mosaic in a patient with achromatopsia associated with a GNAT2 variant","volume":"61","author":"Ueno","year":"2017","journal-title":"Jpn J Ophthalmol"},{"issue":"2","key":"10.1016\/j.ajo.2020.05.016_bib29","doi-asserted-by":"crossref","first-page":"821","DOI":"10.1167\/iovs.16-20427","article-title":"The clinical phenotype of CNGA3-related achromatopsia: pretreatment characterization in preparation of a gene replacement therapy trial","volume":"58","author":"Zobor","year":"2017","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"3","key":"10.1016\/j.ajo.2020.05.016_bib30","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1016\/j.ajhg.2012.07.006","article-title":"A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia","volume":"91","author":"Kohl","year":"2012","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ajo.2020.05.016_bib31","first-page":"876","article-title":"Blue cone monochromacy: causative mutations and associated phenotypes","volume":"15","author":"Gardner","year":"2009","journal-title":"Mol Vis"},{"issue":"13","key":"10.1016\/j.ajo.2020.05.016_bib32","doi-asserted-by":"crossref","first-page":"8006","DOI":"10.1167\/iovs.12-11087","article-title":"The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic","volume":"53","author":"Carroll","year":"2012","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"10","key":"10.1016\/j.ajo.2020.05.016_bib33","doi-asserted-by":"crossref","first-page":"4238","DOI":"10.1167\/iovs.18-24699","article-title":"Residual cone structure in patients with X-linked cone opsin mutations","volume":"59","author":"Patterson","year":"2018","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib34","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1097\/IAE.0000000000000659","article-title":"Insights into autosomal dominant Stargardt-like macular dystrophy through multimodality diagnostic imaging","volume":"36","author":"Palejwala","year":"2016","journal-title":"Retina"},{"issue":"9","key":"10.1016\/j.ajo.2020.05.016_bib35","doi-asserted-by":"crossref","first-page":"6416","DOI":"10.1167\/iovs.12-11550","article-title":"Characterization of Stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging","volume":"54","author":"Ritter","year":"2013","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"8","key":"10.1016\/j.ajo.2020.05.016_bib36","doi-asserted-by":"crossref","first-page":"1567","DOI":"10.1097\/IAE.0000000000000136","article-title":"Multimodal imaging and multifocal electroretinography demonstrate autosomal recessive Stargardt disease may present like occult macular dystrophy","volume":"34","author":"Sisk","year":"2014","journal-title":"Retina"},{"issue":"7","key":"10.1016\/j.ajo.2020.05.016_bib37","doi-asserted-by":"crossref","first-page":"3673","DOI":"10.1167\/iovs.09-4169","article-title":"Morphologic photoreceptor abnormality in occult macular dystrophy on spectral-domain optical coherence tomography","volume":"51","author":"Park","year":"2010","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"7","key":"10.1016\/j.ajo.2020.05.016_bib38","doi-asserted-by":"crossref","first-page":"880","DOI":"10.1001\/jamaophthalmol.2013.172","article-title":"Multimodal imaging of occult macular dystrophy","volume":"131","author":"Ahn","year":"2013","journal-title":"JAMA Ophthalmol"},{"issue":"14","key":"10.1016\/j.ajo.2020.05.016_bib39","doi-asserted-by":"crossref","first-page":"6020","DOI":"10.1167\/iovs.17-21969","article-title":"Parafoveal photoreceptor abnormalities in asymptomatic patients with RP1L1 mutations in families with occult macular dystrophy","volume":"58","author":"Kato","year":"2017","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"10.1016\/j.ajo.2020.05.016_bib40","doi-asserted-by":"crossref","DOI":"10.1136\/bcr-2016-218364","article-title":"ERG and OCT findings of a patient with a clinical diagnosis of occult macular dystrophy in a patient of Ashkenazi Jewish descent associated with a novel mutation in the gene encoding RP1L1","volume":"2017","author":"Saffra","year":"2017","journal-title":"BMJ Case Rep"},{"issue":"2","key":"10.1016\/j.ajo.2020.05.016_bib41","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1136\/bjo.2011.203638","article-title":"High-resolution optical coherence tomography imaging in KCNV2 retinopathy","volume":"96","author":"Sergouniotis","year":"2012","journal-title":"Br J Ophthalmol"},{"issue":"4","key":"10.1016\/j.ajo.2020.05.016_bib42","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1038\/eye.2014.7","article-title":"A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D gene","volume":"28","author":"Mukherjee","year":"2014","journal-title":"Eye (Lond)"},{"key":"10.1016\/j.ajo.2020.05.016_bib43","first-page":"198","article-title":"Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations","volume":"23","author":"Manes","year":"2017","journal-title":"Mol Vis"},{"issue":"3","key":"10.1016\/j.ajo.2020.05.016_bib44","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1055\/s-0035-1545702","article-title":"Genotype-phenotype correlation in patients with PRPH2-mutations [in German]","volume":"232","author":"Maertz","year":"2015","journal-title":"Klin Monbl Augenheilkd"},{"issue":"2","key":"10.1016\/j.ajo.2020.05.016_bib45","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1016\/j.ajhg.2014.06.012","article-title":"Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy","volume":"95","author":"Roosing","year":"2014","journal-title":"Am J Hum Genet"},{"issue":"3","key":"10.1016\/j.ajo.2020.05.016_bib46","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1097\/ICB.0b013e31828ef084","article-title":"Circumscribed outer foveolar defects in spinocerebellar ataxia type 7","volume":"7","author":"Watkins","year":"2013","journal-title":"Retin Cases Brief Rep"},{"issue":"6","key":"10.1016\/j.ajo.2020.05.016_bib47","doi-asserted-by":"crossref","first-page":"1291","DOI":"10.1016\/j.ajo.2014.02.046","article-title":"Pseudocystic foveal cavitation in tamoxifen retinopathy","volume":"157","author":"Doshi","year":"2014","journal-title":"Am J Ophthalmol"},{"issue":"8","key":"10.1016\/j.ajo.2020.05.016_bib48","doi-asserted-by":"crossref","first-page":"681","DOI":"10.1016\/j.oret.2019.03.014","article-title":"Optical coherence tomography angiographic findings of tamoxifen retinopathy: similarity with macular telangiectasia type 2","volume":"3","author":"Lee","year":"2019","journal-title":"Ophthalmol Retina"},{"issue":"11","key":"10.1016\/j.ajo.2020.05.016_bib49","doi-asserted-by":"crossref","first-page":"1479","DOI":"10.1038\/eye.2012.191","article-title":"Adverse ophthalmic reaction in poppers users: case series of \u2018poppers maculopathy\u2019","volume":"26","author":"Davies","year":"2012","journal-title":"Eye (Lond)"},{"issue":"6","key":"10.1016\/j.ajo.2020.05.016_bib50","doi-asserted-by":"crossref","first-page":"888","DOI":"10.1038\/eye.2012.37","article-title":"\u2018Poppers maculopathy\u2019\u2014an emerging ophthalmic reaction to recreational substance abuse","volume":"26","author":"Davies","year":"2012","journal-title":"Eye (Lond)"},{"key":"10.1016\/j.ajo.2020.05.016_bib51","doi-asserted-by":"crossref","DOI":"10.1136\/bcr-2016-214442","article-title":"Poppers retinopathy","volume":"2016","author":"Luis","year":"2016","journal-title":"BMJ Case Rep"},{"key":"10.1016\/j.ajo.2020.05.016_bib52","first-page":"2127","article-title":"Bilateral macular injury from a green laser pointer","volume":"7","author":"Dirani","year":"2013","journal-title":"Clin Ophthalmol"},{"issue":"1","key":"10.1016\/j.ajo.2020.05.016_bib53","doi-asserted-by":"crossref","first-page":"59","DOI":"10.3109\/13816810.2015.1059458","article-title":"Laser-induced photic injury phenocopies macular dystrophy","volume":"37","author":"Zhang","year":"2016","journal-title":"Ophthalmic Genet"},{"issue":"49","key":"10.1016\/j.ajo.2020.05.016_bib54","first-page":"831","article-title":"Retinal injury following laser pointer exposure","volume":"114","author":"Birtel","year":"2017","journal-title":"Dtsch Arztebl Int"},{"issue":"9","key":"10.1016\/j.ajo.2020.05.016_bib55","doi-asserted-by":"crossref","first-page":"1340","DOI":"10.1097\/IAE.0b013e3181b0da88","article-title":"Solar retinopathy: comparison of optical coherence tomography (OCT) and fluorescein angiography (FA)","volume":"29","author":"Jain","year":"2009","journal-title":"Retina"},{"issue":"5","key":"10.1016\/j.ajo.2020.05.016_bib56","doi-asserted-by":"crossref","first-page":"1081","DOI":"10.1007\/s10792-018-0919-x","article-title":"Predictive value of spectral-domain optical coherence tomography features in assessment of visual prognosis in eyes with acute welding arc maculopathy","volume":"39","author":"Zhang","year":"2019","journal-title":"Int Ophthalmol"}],"container-title":["American Journal of Ophthalmology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0002939420302464?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0002939420302464?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,11]],"date-time":"2025-09-11T13:43:00Z","timestamp":1757598180000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0002939420302464"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,10]]},"references-count":56,"alternative-id":["S0002939420302464"],"URL":"https:\/\/doi.org\/10.1016\/j.ajo.2020.05.016","relation":{},"ISSN":["0002-9394"],"issn-type":[{"value":"0002-9394","type":"print"}],"subject":[],"published":{"date-parts":[[2020,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy","name":"articletitle","label":"Article Title"},{"value":"American Journal of Ophthalmology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ajo.2020.05.016","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}