{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T13:25:31Z","timestamp":1791293131454,"version":"4.1.0"},"reference-count":9,"publisher":"SAGE Publications","issue":"7","license":[{"start":{"date-parts":[[2005,7,1]],"date-time":"2005-07-01T00:00:00Z","timestamp":1120176000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Child Neurol"],"published-print":{"date-parts":[[2005,7]]},"abstract":"<jats:p>Ataxia and oculomotor apraxia are seen in ataxia-telangiectasia, type 1 ataxia with oculomotor apraxia, and type 2 ataxia with oculomotor apraxia; however, only type 1 ataxia with oculomotor apraxia is associated with aprataxin gene mutation. We report two American children, a sister and a brother, with type 1 ataxia with oculomotor apraxia and aprataxin gene mutations and briefly review type 1 ataxia with oculomotor apraxia. ( J Child Neurol 2005;20:6190\u2014620).<\/jats:p>","DOI":"10.1177\/08830738050200071701","type":"journal-article","created":{"date-parts":[[2017,7,9]],"date-time":"2017-07-09T14:18:11Z","timestamp":1499609891000},"page":"619-620","source":"Crossref","is-referenced-by-count":10,"title":["Type 1 Ataxia With Oculomotor Apraxia With Aprataxin Gene Mutations in Two American Children"],"prefix":"10.1177","volume":"20","author":[{"given":"Chang Y.","family":"Tsao","sequence":"first","affiliation":[{"name":"Department of Pediatrics and Neurology The Ohio State University, ."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"George","family":"Paulson","sequence":"additional","affiliation":[{"name":"Department of Neurology The Ohio State University Columbus, Ohio"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2005,7,1]]},"reference":[{"key":"atypb1","doi-asserted-by":"publisher","DOI":"10.1038\/ng1001-189"},{"key":"atypb2","doi-asserted-by":"publisher","DOI":"10.1038\/ng1001-184"},{"key":"atypb3","doi-asserted-by":"publisher","DOI":"10.1086\/318191"},{"key":"atypb4","doi-asserted-by":"publisher","DOI":"10.1038\/sj.ejhg.5200586"},{"key":"atypb5","first-page":"1320","volume":"67","author":"Nemeth AH","year":"2000","journal-title":"Am J Hum Genet"},{"key":"atypb6","doi-asserted-by":"publisher","DOI":"10.1002\/ana.10808"},{"key":"atypb7","doi-asserted-by":"publisher","DOI":"10.1212\/01.WNL.0000048562.88536.A4"},{"key":"atypb8","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/awg283"},{"key":"atypb9","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.58.2.201"}],"container-title":["Journal of Child Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/08830738050200071701","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/08830738050200071701","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T20:32:29Z","timestamp":1777494749000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/08830738050200071701"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,7]]},"references-count":9,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2005,7]]}},"alternative-id":["10.1177\/08830738050200071701"],"URL":"https:\/\/doi.org\/10.1177\/08830738050200071701","relation":{},"ISSN":["0883-0738","1708-8283"],"issn-type":[{"value":"0883-0738","type":"print"},{"value":"1708-8283","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,7]]}}}