{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T04:56:22Z","timestamp":1764996982070},"reference-count":7,"publisher":"Elsevier BV","issue":"1","content-domain":{"domain":["jocn-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Clinical Neuroscience"],"published-print":{"date-parts":[[2014,1]]},"DOI":"10.1016\/j.jocn.2013.03.016","type":"journal-article","created":{"date-parts":[[2013,6,17]],"date-time":"2013-06-17T08:01:35Z","timestamp":1371456095000},"page":"175-178","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":14,"title":["Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt\u2013Jakob disease"],"prefix":"10.1016","volume":"21","author":[{"given":"Hongliang","family":"Zhang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Meibo","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Limin","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Haining","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tao","family":"Jin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jiang","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Li","family":"Sun","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jocn.2013.03.016_b0005","doi-asserted-by":"crossref","first-page":"340","DOI":"10.1086\/505215","article-title":"Creutzfeldt-Jakob disease: a rare cause of dementia in elderly persons","volume":"43","author":"Knight","year":"2006","journal-title":"Clin Infect Dis"},{"key":"10.1016\/j.jocn.2013.03.016_b0010","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1002\/ana.410050212","article-title":"Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering","volume":"5","author":"Masters","year":"1979","journal-title":"Ann Neurol"},{"key":"10.1016\/j.jocn.2013.03.016_b0015","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/128_2011_157","article-title":"Genetics of prion disease","volume":"305","author":"Lloyd","year":"2011","journal-title":"Top Curr Chem"},{"key":"10.1016\/j.jocn.2013.03.016_b0020","doi-asserted-by":"crossref","first-page":"1673","DOI":"10.1016\/S0140-6736(99)01342-2","article-title":"Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease","volume":"353","author":"Alperovitch","year":"1999","journal-title":"Lancet"},{"key":"10.1016\/j.jocn.2013.03.016_b0025","first-page":"68","article-title":"Association of the PRNP regulatory region polymorphisms with the occurrence of sporadic Creutzfeldt-Jakob disease","volume":"50","author":"Bratosiewicz-W\u0105sik","year":"2012","journal-title":"Folia Neuropathol"},{"key":"10.1016\/j.jocn.2013.03.016_b0030","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1097\/GIM.0b013e3181cd7374","article-title":"The genetics of prion diseases","volume":"12","author":"Mastrianni","year":"2010","journal-title":"Genet Med"},{"key":"10.1016\/j.jocn.2013.03.016_b0035","doi-asserted-by":"crossref","first-page":"618","DOI":"10.1016\/S1474-4422(12)70063-7","article-title":"Sporadic human prion diseases: molecular insights and diagnosis","volume":"11","author":"Puoti","year":"2012","journal-title":"Lancet Neurol"}],"container-title":["Journal of Clinical Neuroscience"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586813002506?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0967586813002506?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,10,15]],"date-time":"2018-10-15T02:56:08Z","timestamp":1539572168000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0967586813002506"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,1]]},"references-count":7,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2014,1]]}},"alternative-id":["S0967586813002506"],"URL":"https:\/\/doi.org\/10.1016\/j.jocn.2013.03.016","relation":{},"ISSN":["0967-5868"],"issn-type":[{"value":"0967-5868","type":"print"}],"subject":[],"published":{"date-parts":[[2014,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt\u2013Jakob disease","name":"articletitle","label":"Article Title"},{"value":"Journal of Clinical Neuroscience","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jocn.2013.03.016","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2013 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}