{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T00:17:38Z","timestamp":1790468258606,"version":"4.1.0"},"reference-count":26,"publisher":"Elsevier BV","issue":"11","license":[{"start":{"date-parts":[[2019,11,1]],"date-time":"2019-11-01T00:00:00Z","timestamp":1572566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,11,1]],"date-time":"2019-11-01T00:00:00Z","timestamp":1572566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/100009619","name":"Japan Agency for Medical Research and Development","doi-asserted-by":"publisher","award":["18ek0109213h0001"],"award-info":[{"award-number":["18ek0109213h0001"]}],"id":[{"id":"10.13039\/100009619","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100009619","name":"Japan Agency for Medical Research and Development","doi-asserted-by":"publisher","award":["JP181k1403004"],"award-info":[{"award-number":["JP181k1403004"]}],"id":[{"id":"10.13039\/100009619","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["aaojournal.org","clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Ophthalmology"],"published-print":{"date-parts":[[2019,11]]},"DOI":"10.1016\/j.ophtha.2019.05.027","type":"journal-article","created":{"date-parts":[[2019,6,6]],"date-time":"2019-06-06T02:18:09Z","timestamp":1559787489000},"page":"1557-1566","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":41,"title":["Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations"],"prefix":"10.1016","volume":"126","author":[{"given":"Koji M.","family":"Nishiguchi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasuhiro","family":"Ikeda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kosuke","family":"Fujita","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hiroshi","family":"Kunikata","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Makoto","family":"Akiho","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kazuki","family":"Hashimoto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katsuhiro","family":"Hosono","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kentaro","family":"Kurata","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshito","family":"Koyanagi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Masato","family":"Akiyama","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Takefumi","family":"Suzuki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ryo","family":"Kawasaki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuko","family":"Wada","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshihiro","family":"Hotta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Koh-Hei","family":"Sonoda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Akira","family":"Murakami","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mitsuru","family":"Nakazawa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Toru","family":"Nakazawa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Toshiaki","family":"Abe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.ophtha.2019.05.027_bib1","first-page":"123","article-title":"On a type of night-blindness","volume":"11","author":"Oguchi","year":"1907","journal-title":"Acta Soc Ophthalmol Jpn"},{"key":"10.1016\/j.ophtha.2019.05.027_bib2","first-page":"1148","article-title":"A\u00a0new discovery in dark adaptation in Oguchi disease","volume":"17","author":"Mizuo","year":"1913","journal-title":"Acta Soc Ophthalmol Jpn"},{"key":"10.1016\/j.ophtha.2019.05.027_bib3","series-title":"Electrodiagnosis of Retinal Diseases","first-page":"119","article-title":"Oguchi\u2019s disease","author":"Miyake","year":"2006"},{"issue":"4","key":"10.1016\/j.ophtha.2019.05.027_bib4","first-page":"511","article-title":"Electrophysiological findings in patients with Oguchi\u2019s disease","volume":"40","author":"Miyake","year":"1996","journal-title":"Jpn J Ophthalmol"},{"issue":"8","key":"10.1016\/j.ophtha.2019.05.027_bib5","first-page":"557","article-title":"Symposium on electrophysiology: electroretinography: some basic principles","volume":"9","author":"Gouras","year":"1970","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"3","key":"10.1016\/j.ophtha.2019.05.027_bib6","doi-asserted-by":"crossref","first-page":"360","DOI":"10.1038\/ng0795-360","article-title":"A\u00a0homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese","volume":"10","author":"Fuchs","year":"1995","journal-title":"Nat Genet"},{"issue":"7","key":"10.1016\/j.ophtha.2019.05.027_bib7","doi-asserted-by":"crossref","first-page":"1410","DOI":"10.1016\/j.ophtha.2003.11.006","article-title":"Novel mutations in the arrestin gene and associated clinical features in Japanese patients with Oguchi\u2019s disease","volume":"111","author":"Nakamura","year":"2004","journal-title":"Ophthalmology"},{"issue":"2","key":"10.1016\/j.ophtha.2019.05.027_bib8","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1038\/ng0297-175","article-title":"Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness","volume":"15","author":"Yamamoto","year":"1997","journal-title":"Nat Genet"},{"issue":"5","key":"10.1016\/j.ophtha.2019.05.027_bib9","doi-asserted-by":"crossref","first-page":"1710","DOI":"10.1021\/bi00405a049","article-title":"Inactivation of photoexcited rhodopsin in retinal rods: the roles of rhodopsin kinase and 48-kDa protein (arrestin)","volume":"27","author":"Bennett","year":"1988","journal-title":"Biochemistry"},{"issue":"4","key":"10.1016\/j.ophtha.2019.05.027_bib10","doi-asserted-by":"crossref","first-page":"498","DOI":"10.1001\/archopht.116.4.498","article-title":"Arrestin gene mutations in autosomal recessive retinitis pigmentosa","volume":"116","author":"Nakazawa","year":"1998","journal-title":"Arch Ophthalmol"},{"issue":"2","key":"10.1016\/j.ophtha.2019.05.027_bib11","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1016\/S0002-9394(99)80100-7","article-title":"Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene","volume":"125","author":"Nakamachi","year":"1998","journal-title":"Am J Ophthalmol"},{"issue":"6","key":"10.1016\/j.ophtha.2019.05.027_bib12","doi-asserted-by":"crossref","first-page":"394","DOI":"10.1159\/000055501","article-title":"Visual function and gene analysis in a family with Oguchi\u2019s disease","volume":"30","author":"Yoshii","year":"1998","journal-title":"Ophthalmic Res"},{"issue":"10","key":"10.1016\/j.ophtha.2019.05.027_bib13","doi-asserted-by":"crossref","first-page":"1197","DOI":"10.1136\/bjo.83.10.1194d","article-title":"Retinitis pigmentosa with visual fluctuation and arrestin gene mutation","volume":"83","author":"Isashiki","year":"1999","journal-title":"Br J Ophthalmol"},{"issue":"2","key":"10.1016\/j.ophtha.2019.05.027_bib14","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1007\/s10633-011-9286-x","article-title":"Oguchi disease masked by retinitis pigmentosa","volume":"123","author":"Sonoyama","year":"2011","journal-title":"Doc Ophthalmol"},{"issue":"1","key":"10.1016\/j.ophtha.2019.05.027_bib15","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1097\/00006982-199701000-00004","article-title":"Oguchi disease: phenotypic characteristics of patients with the frequent 1147delA mutation in the arrestin gene","volume":"17","author":"Nakazawa","year":"1997","journal-title":"Retina"},{"issue":"S1","key":"10.1016\/j.ophtha.2019.05.027_bib16","doi-asserted-by":"crossref","first-page":"S317","DOI":"10.1002\/humu.1380110199","article-title":"Two Indian siblings with Oguchi disease are homozygous for an arrestin mutation encoding premature termination","volume":"11","author":"Maw","year":"1998","journal-title":"Hum Mutat"},{"issue":"4","key":"10.1016\/j.ophtha.2019.05.027_bib17","doi-asserted-by":"crossref","first-page":"2162","DOI":"10.1167\/iovs.14-16198","article-title":"Association of retinal artery and other inner retinal structures with distribution of tapetal-like reflex in Oguchi\u2019s disease","volume":"56","author":"Kato","year":"2015","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"1","key":"10.1016\/j.ophtha.2019.05.027_bib18","doi-asserted-by":"crossref","first-page":"134","DOI":"10.1016\/j.ophtha.2006.05.069","article-title":"A\u00a0novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses","volume":"114","author":"Hayashi","year":"2007","journal-title":"Ophthalmology"},{"issue":"3","key":"10.1016\/j.ophtha.2019.05.027_bib19","doi-asserted-by":"crossref","first-page":"329","DOI":"10.1001\/archopht.1994.01090150059023","article-title":"Functional status and quality of life measurement among ophthalmic patients","volume":"112","author":"Scott","year":"1994","journal-title":"Arch Ophthalmol"},{"issue":"1","key":"10.1016\/j.ophtha.2019.05.027_bib20","first-page":"95","article-title":"Conversion of planimetric visual field data into solid angles and retinal areas","volume":"5","author":"Dagnelie","year":"1990","journal-title":"Clin Vision Sci"},{"issue":"1","key":"10.1016\/j.ophtha.2019.05.027_bib21","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":"7","key":"10.1016\/j.ophtha.2019.05.027_bib22","doi-asserted-by":"crossref","first-page":"874","DOI":"10.1001\/jamaophthalmol.2014.849","article-title":"Ophthalmologic examinations in areas of Miyagi Prefecture affected by the Great East Japan Earthquake","volume":"132","author":"Doi","year":"2014","journal-title":"JAMA Ophthalmol"},{"issue":"6","key":"10.1016\/j.ophtha.2019.05.027_bib23","doi-asserted-by":"crossref","first-page":"658","DOI":"10.1136\/bjo.86.6.658","article-title":"Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia","volume":"86","author":"Roberts","year":"2002","journal-title":"Br J Ophthalmol"},{"key":"10.1016\/j.ophtha.2019.05.027_bib24","first-page":"121","article-title":"Report of a patient with Oguchi disease","volume":"48","author":"Majima","year":"1954","journal-title":"Jpn Rev Clin Ophthalmology"},{"issue":"4","key":"10.1016\/j.ophtha.2019.05.027_bib25","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1159\/000325024","article-title":"Macular dysfunction in Oguchi disease with the frequent mutation 1147delA in the SAG gene","volume":"46","author":"Hayashi","year":"2011","journal-title":"Ophthalmic Res"},{"issue":"11","key":"10.1016\/j.ophtha.2019.05.027_bib26","doi-asserted-by":"crossref","first-page":"1561","DOI":"10.1007\/s00417-009-1114-6","article-title":"Shortening of the rod outer segment in Oguchi disease","volume":"247","author":"Hashimoto","year":"2009","journal-title":"Graefes Arch Clin Exp Ophthalmol"}],"container-title":["Ophthalmology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0161642019307250?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0161642019307250?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T19:52:42Z","timestamp":1777492362000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0161642019307250"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,11]]},"references-count":26,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2019,11]]}},"alternative-id":["S0161642019307250"],"URL":"https:\/\/doi.org\/10.1016\/j.ophtha.2019.05.027","relation":{},"ISSN":["0161-6420"],"issn-type":[{"value":"0161-6420","type":"print"}],"subject":[],"published":{"date-parts":[[2019,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations","name":"articletitle","label":"Article Title"},{"value":"Ophthalmology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ophtha.2019.05.027","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 by the American Academy of Ophthalmology","name":"copyright","label":"Copyright"}]}}