{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,2,21]],"date-time":"2025-02-21T04:57:20Z","timestamp":1740113840892,"version":"3.37.3"},"reference-count":6,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,9,1]],"date-time":"2017-09-01T00:00:00Z","timestamp":1504224000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/501100004085","name":"Ministry of Education, Science and Technology","doi-asserted-by":"publisher","award":["NRF-2010-0014167"],"award-info":[{"award-number":["NRF-2010-0014167"]}],"id":[{"id":"10.13039\/501100004085","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003725","name":"National Research Foundation of Korea","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100003725","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.fr","clinicalkey.jp","clinicalkey.com.au","clinicalkey.es","clinicalkey.com","jns-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of the Neurological Sciences"],"published-print":{"date-parts":[[2017,9]]},"DOI":"10.1016\/j.jns.2017.07.017","type":"journal-article","created":{"date-parts":[[2017,7,10]],"date-time":"2017-07-10T17:45:26Z","timestamp":1499708726000},"page":"174-176","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"special_numbering":"C","title":["MtDNA m.3472T &gt; C could be classified as a primary mutation of Leber's hereditary optic neuropathy"],"prefix":"10.1016","volume":"380","author":[{"given":"Moon-Woo","family":"Seong","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jongmoon","family":"Choi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sung Sup","family":"Park","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ji Yeon","family":"Kim","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jeong-Min","family":"Hwang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jns.2017.07.017_bb0005","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1086\/346066","article-title":"The epidemiology of Leber hereditary optic neuropathy in the north east of England","volume":"72","author":"Yu-Wai-Man","year":"2003","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.jns.2017.07.017_bb0010","doi-asserted-by":"crossref","first-page":"630","DOI":"10.1002\/ana.10177","article-title":"Mitochondrial DNA C4171A\/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis","volume":"51","author":"Kim","year":"2002","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.jns.2017.07.017_bb0020","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1111\/ceo.12355","article-title":"New MT-ND1 pathologic mutation for Leber hereditary optic neuropathy","volume":"42","author":"Mart\u00ednez-Romero","year":"2014","journal-title":"Clin. Exp. Ophthalmol."},{"key":"10.1016\/j.jns.2017.07.017_bb0025","doi-asserted-by":"crossref","first-page":"748","DOI":"10.1134\/S0006297916070117","article-title":"Previously unclassified mutation of mtDNA m.3472T>C: evidence of pathogenicity in Leber's hereditary optic neuropathy","volume":"81","author":"Sheremet","year":"2016","journal-title":"Biochemistry (Mosc)"},{"key":"10.1016\/j.jns.2017.07.017_bb0030","doi-asserted-by":"crossref","first-page":"2377","DOI":"10.1167\/iovs.16-19243","article-title":"Mitochondrial ND1 variants in 1281 Chinese subjects with Leber's hereditary optic neuropathy","volume":"57","author":"Ji","year":"2016","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.jns.2017.07.017_bb0035","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1007\/s00415-003-0985-4","article-title":"Spectrum of the mitochondrial DNA mutations of Leber's hereditary optic neuropathy in Koreans","volume":"250","author":"Kim","year":"2003","journal-title":"J. Neurol."}],"container-title":["Journal of the Neurological Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X17304513?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X17304513?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2022,6,24]],"date-time":"2022-06-24T03:37:10Z","timestamp":1656041830000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022510X17304513"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,9]]},"references-count":6,"alternative-id":["S0022510X17304513"],"URL":"https:\/\/doi.org\/10.1016\/j.jns.2017.07.017","relation":{},"ISSN":["0022-510X"],"issn-type":[{"type":"print","value":"0022-510X"}],"subject":[],"published":{"date-parts":[[2017,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"MtDNA m.3472T>C could be classified as a primary mutation of Leber's hereditary optic neuropathy","name":"articletitle","label":"Article Title"},{"value":"Journal of the Neurological Sciences","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jns.2017.07.017","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}