{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T17:50:51Z","timestamp":1786989051785,"version":"build-2736575974"},"reference-count":50,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,5,21]],"date-time":"2023-05-21T00:00:00Z","timestamp":1684627200000},"content-version":"am","delay-in-days":324,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2022,7,1]],"date-time":"2022-07-01T00:00:00Z","timestamp":1656633600000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["K08EY030950"],"award-info":[{"award-number":["K08EY030950"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["K12-EY015398"],"award-info":[{"award-number":["K12-EY015398"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["P30-EY001583"],"award-info":[{"award-number":["P30-EY001583"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R01-EY006855"],"award-info":[{"award-number":["R01-EY006855"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R01-EY019304"],"award-info":[{"award-number":["R01-EY019304"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R01-EY025752"],"award-info":[{"award-number":["R01-EY025752"]}],"id":[{"id":"10.13039\/100000002","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\/100001818","name":"Research to Prevent Blindness","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001818","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100006920","name":"University of Pennsylvania","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100006920","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Experimental Eye Research"],"published-print":{"date-parts":[[2022,7]]},"DOI":"10.1016\/j.exer.2022.109106","type":"journal-article","created":{"date-parts":[[2022,5,16]],"date-time":"2022-05-16T17:41:40Z","timestamp":1652722900000},"page":"109106","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"special_numbering":"C","title":["Quantitative and qualitative characterization of retinal dystrophies in canine models of inherited retinal diseases using spectral domain optical coherence tomography (SD-OCT)"],"prefix":"10.1016","volume":"220","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3128-2760","authenticated-orcid":false,"given":"Shin Ae","family":"Park","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jamie","family":"Rhodes","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Simone","family":"Iwabe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gui-Shuang","family":"Ying","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wei","family":"Pan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jiayan","family":"Huang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8845-0588","authenticated-orcid":false,"given":"Andr\u00e1s M.","family":"Kom\u00e1romy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.exer.2022.109106_bib1","doi-asserted-by":"crossref","first-page":"1072","DOI":"10.1016\/j.ymthe.2005.08.008","article-title":"Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness","volume":"12","author":"Acland","year":"2005","journal-title":"Mol. Ther. : J.Am.Soc.Gene Ther."},{"key":"10.1016\/j.exer.2022.109106_bib2","doi-asserted-by":"crossref","first-page":"92","DOI":"10.1038\/ng0501-92","article-title":"Gene therapy restores vision in a canine model of childhood blindness","volume":"28","author":"Acland","year":"2001","journal-title":"Nat. Genet."},{"key":"10.1016\/j.exer.2022.109106_bib3","doi-asserted-by":"crossref","first-page":"625","DOI":"10.1016\/S0014-4835(82)80075-4","article-title":"Retinal degeneration in the dog. III. Abnormal cyclic nucleotide metabolism in rod-cone dysplasia","volume":"35","author":"Aguirre","year":"1982","journal-title":"Exp. Eye Res."},{"key":"10.1016\/j.exer.2022.109106_bib4","doi-asserted-by":"crossref","first-page":"663","DOI":"10.1016\/S0014-4835(88)80055-1","article-title":"Variation in retinal degeneration phenotype inherited at the prcd locus","volume":"46","author":"Aguirre","year":"1988","journal-title":"Exp. Eye Res."},{"key":"10.1016\/j.exer.2022.109106_bib5","doi-asserted-by":"crossref","first-page":"4759","DOI":"10.1167\/iovs.07-0453","article-title":"Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations","volume":"48","author":"Aleman","year":"2007","journal-title":"Investig. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.exer.2022.109106_bib6","doi-asserted-by":"crossref","first-page":"883","DOI":"10.1089\/hum.2013.146","article-title":"Successful gene therapy in older Rpe65-deficient dogs following subretinal injection of an adeno-associated vector expressing RPE65","volume":"24","author":"Annear","year":"2013","journal-title":"Hum. Gene Ther."},{"key":"10.1016\/j.exer.2022.109106_bib7","doi-asserted-by":"crossref","DOI":"10.3390\/cells10010115","article-title":"A comprehensive study of the retinal phenotype of Rpe65-deficient dogs","volume":"10","author":"Annear","year":"2021","journal-title":"Cells"},{"key":"10.1016\/j.exer.2022.109106_bib8","doi-asserted-by":"crossref","first-page":"1887","DOI":"10.1056\/NEJMoa1414221","article-title":"Long-term effect of gene therapy on Leber's congenital amaurosis","volume":"372","author":"Bainbridge","year":"2015","journal-title":"N. Engl. J. Med."},{"key":"10.1016\/j.exer.2022.109106_bib9","series-title":"Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie","article-title":"Correlation of SD-OCT findings and visual function in patients with retinitis pigmentosa","author":"Battaglia Parodi","year":"2015"},{"key":"10.1016\/j.exer.2022.109106_bib10","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0090390","article-title":"Canine retina has a primate fovea-like bouquet of cone photoreceptors which is affected by inherited macular degenerations","volume":"9","author":"Beltran","year":"2014","journal-title":"PLoS One"},{"key":"10.1016\/j.exer.2022.109106_bib11","doi-asserted-by":"crossref","first-page":"1669","DOI":"10.1167\/iovs.05-0845","article-title":"A frameshift mutation in RPGR exon ORF15 causes photoreceptor degeneration and inner retina remodeling in a model of X-linked retinitis pigmentosa","volume":"47","author":"Beltran","year":"2006","journal-title":"Investig. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.exer.2022.109106_bib12","doi-asserted-by":"crossref","first-page":"1074","DOI":"10.1002\/humu.20565","article-title":"Centrosomal-ciliary gene CEP290\/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis","volume":"28","author":"Cideciyan","year":"2007","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.exer.2022.109106_bib13","doi-asserted-by":"crossref","first-page":"E517","DOI":"10.1073\/pnas.1218933110","article-title":"Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement","volume":"110","author":"Cideciyan","year":"2013","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"10.1016\/j.exer.2022.109106_bib14","first-page":"1299","article-title":"Histology of the normal collie eye. III. Lens, retina and optic nerve","volume":"6","author":"Donovan","year":"1974","journal-title":"Ann. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib15","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1016\/j.ajhg.2010.06.016","article-title":"Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesterase","volume":"87","author":"Dvir","year":"2010","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.exer.2022.109106_bib16","doi-asserted-by":"crossref","first-page":"266","DOI":"10.1016\/j.ymthe.2019.08.013","article-title":"Long-Term structural outcomes of late-stage RPE65 gene therapy","volume":"28","author":"Gardiner","year":"2020","journal-title":"Mol. Ther. : J.Am.Soc.Gene Ther."},{"key":"10.1016\/j.exer.2022.109106_bib17","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.ajo.2018.04.025","article-title":"Ellipsoid zone change according to Glaucoma stage advancement","volume":"192","author":"Ha","year":"2018","journal-title":"Am. J. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib18","doi-asserted-by":"crossref","first-page":"400","DOI":"10.1111\/j.1463-5224.2011.00887.x","article-title":"Spectral domain optical coherence tomography (SD-OCT) assessment of the healthy female canine retina and optic nerve","volume":"14","author":"Hernandez-Merino","year":"2011","journal-title":"Vet. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib19","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1080\/13816810.2017.1418389","article-title":"Achromatopsia: clinical features, molecular genetics, animal models and therapeutic options","volume":"39","author":"Hirji","year":"2018","journal-title":"Ophthalmic Genet."},{"key":"10.1016\/j.exer.2022.109106_bib20","doi-asserted-by":"crossref","first-page":"169","DOI":"10.1007\/978-3-319-17121-0_23","article-title":"Leber congenital amaurosis: Genotypes and retinal structure phenotypes","volume":"854","author":"Jacobson","year":"2016","journal-title":"Adv. Exp. Med. Biol."},{"issue":"2","key":"10.1016\/j.exer.2022.109106_bib21","doi-asserted-by":"crossref","first-page":"256","DOI":"10.1136\/bjophthalmol-2020-317692","article-title":"Inner retinal thickening affects microperimetry thresholds in the presence of photoreceptor thinning in patients with RPGR retinitis pigmentosa","volume":"106","author":"Jolly","year":"2020","journal-title":"Br. J. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib22","doi-asserted-by":"crossref","first-page":"2581","DOI":"10.1093\/hmg\/ddq136","article-title":"Gene therapy rescues cone function in congenital achromatopsia","volume":"19","author":"Komaromy","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.exer.2022.109106_bib23","doi-asserted-by":"crossref","first-page":"1131","DOI":"10.1038\/mt.2013.50","article-title":"Transient photoreceptor deconstruction by CNTF enhances rAAV-mediated cone functional rescue in late stage CNGB3-achromatopsia","volume":"21","author":"Komaromy","year":"2013","journal-title":"Mol. Ther. : J.Am.Soc.Gene Ther."},{"key":"10.1016\/j.exer.2022.109106_bib24","article-title":"Development of retinal bullae in dogs with progressive retinal atrophy","author":"Marinho","year":"2021","journal-title":"Vet. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib25","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1038\/ng1097-139","article-title":"Mutations in RPE65 cause Leber's congenital amaurosis","volume":"17","author":"Marlhens","year":"1997","journal-title":"Nat. Genet."},{"key":"10.1016\/j.exer.2022.109106_bib26","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1016\/j.exer.2015.06.007","article-title":"RPGR: its role in photoreceptor physiology, human disease, and future therapies","volume":"138","author":"Megaw","year":"2015","journal-title":"Exp. Eye Res."},{"key":"10.1016\/j.exer.2022.109106_bib27","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1016\/j.survophthal.2006.02.007","article-title":"Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis","volume":"51","author":"Michaelides","year":"2006","journal-title":"Surv. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib28","doi-asserted-by":"crossref","first-page":"1","DOI":"10.2152\/jmi.59.1","article-title":"Diagnostic imaging in patients with retinitis pigmentosa","volume":"59","author":"Mitamura","year":"2012","journal-title":"J. Med. Invest. : JMI"},{"key":"10.1016\/j.exer.2022.109106_bib29","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1038\/gt.2012.63","article-title":"RPE65 gene therapy slows cone loss in Rpe65-deficient dogs","volume":"20","author":"Mowat","year":"2013","journal-title":"Gene Ther."},{"key":"10.1016\/j.exer.2022.109106_bib30","doi-asserted-by":"crossref","first-page":"3268","DOI":"10.1167\/iovs.17-21930","article-title":"Early-onset progressive degeneration of the area centralis in RPE65-deficient dogs","volume":"58","author":"Mowat","year":"2017","journal-title":"Investig. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.exer.2022.109106_bib31","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1016\/j.bj.2016.04.003","article-title":"Clinical applications of spectral domain optical coherence tomography in retinal diseases","volume":"39","author":"Murthy","year":"2016","journal-title":"Biomed. J."},{"key":"10.1016\/j.exer.2022.109106_bib32","doi-asserted-by":"crossref","first-page":"485","DOI":"10.3928\/1542-8877-20041101-09","article-title":"Retinal thickness in normal and RCD1 dogs using optical coherence tomography","volume":"35","author":"Panzan","year":"2004","journal-title":"Ophthalmic Surg. Laser. Imag. : Off. J.Int. Soc. Imaging.Eye"},{"key":"10.1016\/j.exer.2022.109106_bib33","doi-asserted-by":"crossref","first-page":"2608","DOI":"10.1167\/iovs.09-3734","article-title":"Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosis","volume":"51","author":"Pasadhika","year":"2010","journal-title":"Investig. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.exer.2022.109106_bib34","first-page":"171","article-title":"ERG assessment of altered retinal function in canine models of retinitis pigmentosa and monitoring of response to translatable gene augmentation therapy. Documenta ophthalmologica","volume":"143","author":"Pasmanter","year":"2021","journal-title":"Adv. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib35","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1111\/j.1748-5827.1995.tb02934.x","article-title":"Incidence of the gene mutation causal for rod-cone dysplasia type 1 in Irish setters in the UK","volume":"36","author":"Petersen-Jones","year":"1995","journal-title":"J. Small Anim. Pract."},{"key":"10.1016\/j.exer.2022.109106_bib36","first-page":"15","article-title":"Dog models for blinding inherited retinal dystrophies. Human gene therapy","volume":"26","author":"Petersen-Jones","year":"2015","journal-title":"Clinical development"},{"key":"10.1016\/j.exer.2022.109106_bib37","doi-asserted-by":"crossref","first-page":"2019","DOI":"10.1038\/mt.2012.134","article-title":"Restoration of vision in the pde6beta-deficient dog, a large animal model of rod-cone dystrophy","volume":"20","author":"Petit","year":"2012","journal-title":"Mol. Ther. : J.Am.Soc.Gene Ther."},{"key":"10.1016\/j.exer.2022.109106_bib38","doi-asserted-by":"crossref","first-page":"702","DOI":"10.1016\/j.ajo.2006.04.057","article-title":"Screening genes of the retinoid metabolism: novel LRAT mutation in leber congenital amaurosis","volume":"142","author":"Senechal","year":"2006","journal-title":"Am. J. Ophthalmol."},{"key":"10.1016\/j.exer.2022.109106_bib39","doi-asserted-by":"crossref","first-page":"1823","DOI":"10.1093\/hmg\/11.16.1823","article-title":"Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3","volume":"11","author":"Sidjanin","year":"2002","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.exer.2022.109106_bib40","doi-asserted-by":"crossref","first-page":"1009","DOI":"10.3928\/23258160-20151027-04","article-title":"Quantitative assessment of retinal degeneration in birdshot chorioretinopathy using optical coherence tomography","volume":"46","author":"Symes","year":"2015","journal-title":"Ophthalmic surgery, lasers & imaging retina"},{"key":"10.1016\/j.exer.2022.109106_bib41","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1167\/iovs.08-2562","article-title":"Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutation","volume":"50","author":"Tuntivanich","year":"2009","journal-title":"Investig. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.exer.2022.109106_bib42","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1006\/geno.1999.5754","article-title":"Retinal dystrophy of Swedish briard\/briard-beagle dogs is due to a 4-bp deletion in RPE65","volume":"57","author":"Veske","year":"1999","journal-title":"Genomics"},{"key":"10.1016\/j.exer.2022.109106_bib43","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1167\/tvst.4.5.8","article-title":"Outer segment thickness predicts visual field response to QLT091001 in patients with or mutations","volume":"4","author":"Wen","year":"2015","journal-title":"Transl Vis Sci Technol"},{"key":"10.1016\/j.exer.2022.109106_bib44","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0072229","article-title":"A large animal model for CNGB1 autosomal recessive retinitis pigmentosa","volume":"8","author":"Winkler","year":"2013","journal-title":"PLoS One"},{"key":"10.1016\/j.exer.2022.109106_bib45","doi-asserted-by":"crossref","DOI":"10.3390\/cells9040882","article-title":"Large animal models of inherited retinal degenerations: a review","volume":"9","author":"Winkler","year":"2020","journal-title":"Cells"},{"key":"10.1016\/j.exer.2022.109106_bib46","doi-asserted-by":"crossref","first-page":"292","DOI":"10.1038\/sj.eye.6701466","article-title":"Relationship of gender, body mass index, and axial length with central retinal thickness using optical coherence tomography","volume":"19","author":"Wong","year":"2005","journal-title":"Eye"},{"key":"10.1016\/j.exer.2022.109106_bib47","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1186\/1471-2156-14-27","article-title":"Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia","volume":"14","author":"Yeh","year":"2013","journal-title":"BMC Genet."},{"key":"10.1016\/j.exer.2022.109106_bib48","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1080\/09286586.2016.1259636","article-title":"Tutorial on biostatistics: linear Regression analysis of continuous correlated eye data","volume":"24","author":"Ying","year":"2017","journal-title":"Ophthalmic Epidemiol."},{"key":"10.1016\/j.exer.2022.109106_bib49","doi-asserted-by":"crossref","first-page":"507","DOI":"10.1111\/cxo.12175","article-title":"Achromatopsia: case presentation and literature review emphasising the value of spectral domain optical coherence tomography","volume":"97","author":"Yu","year":"2014","journal-title":"Clin. Exp. Optom."},{"key":"10.1016\/j.exer.2022.109106_bib50","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1016\/j.ygeno.2006.07.007","article-title":"Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans","volume":"88","author":"Zangerl","year":"2006","journal-title":"Genomics"}],"container-title":["Experimental Eye Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0014483522001865?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0014483522001865?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,16]],"date-time":"2025-09-16T05:21:12Z","timestamp":1758000072000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0014483522001865"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,7]]},"references-count":50,"alternative-id":["S0014483522001865"],"URL":"https:\/\/doi.org\/10.1016\/j.exer.2022.109106","relation":{},"ISSN":["0014-4835"],"issn-type":[{"value":"0014-4835","type":"print"}],"subject":[],"published":{"date-parts":[[2022,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Quantitative and qualitative characterization of retinal dystrophies in canine models of inherited retinal diseases using spectral domain optical coherence tomography (SD-OCT)","name":"articletitle","label":"Article Title"},{"value":"Experimental Eye Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.exer.2022.109106","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2022 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"109106"}}