{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,4,18]],"date-time":"2025-04-18T20:04:34Z","timestamp":1745006674609},"reference-count":27,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2012,5,1]],"date-time":"2012-05-01T00:00:00Z","timestamp":1335830400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neuroscience Letters"],"published-print":{"date-parts":[[2012,5]]},"DOI":"10.1016\/j.neulet.2012.03.097","type":"journal-article","created":{"date-parts":[[2012,4,9]],"date-time":"2012-04-09T19:35:48Z","timestamp":1334000148000},"page":"18-20","source":"Crossref","is-referenced-by-count":5,"title":["Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD"],"prefix":"10.1016","volume":"517","author":[{"given":"Yi","family":"Guo","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiong","family":"Deng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jie","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Linyan","family":"Su","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hongbo","family":"Xu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ziqiang","family":"Luo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hao","family":"Deng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.neulet.2012.03.097_bib0005","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1126\/science.1116502","article-title":"Sequence variants in SLITRK1 are associated with Tourette's syndrome","volume":"310","author":"Abelson","year":"2005","journal-title":"Science"},{"key":"10.1016\/j.neulet.2012.03.097_bib0010","doi-asserted-by":"crossref","first-page":"711","DOI":"10.1038\/sj.ejhg.5201824","article-title":"Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome","volume":"15","author":"Belloso","year":"2007","journal-title":"European Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0015","first-page":"999","article-title":"Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3","volume":"59","author":"Boghosian-Sell","year":"1996","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0020","doi-asserted-by":"crossref","first-page":"361518","DOI":"10.1155\/2009\/361518","article-title":"Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication","volume":"2009","author":"Clarke","year":"2009","journal-title":"Case Report Medicine"},{"key":"10.1016\/j.neulet.2012.03.097_bib0025","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1002\/ajmg.a.30066","article-title":"Candidate locus for Gilles de la Tourette syndrome\/obsessive compulsive disorder\/chronic tic disorder at 18q22","volume":"130A","author":"Cuker","year":"2004","journal-title":"American Journal of Medical Genetics Part A"},{"key":"10.1016\/j.neulet.2012.03.097_bib0030","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1038\/nrneurol.2012.26","article-title":"Genetics of Tourette syndrome","volume":"8","author":"Deng","year":"2012","journal-title":"Nature Reviews of Neurology"},{"key":"10.1016\/j.neulet.2012.03.097_bib0035","doi-asserted-by":"crossref","first-page":"400","DOI":"10.1111\/j.1600-0404.2006.00706.x","article-title":"Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome","volume":"114","author":"Deng","year":"2006","journal-title":"Acta Neurologica Scandinavica"},{"key":"10.1016\/j.neulet.2012.03.097_bib0040","doi-asserted-by":"crossref","first-page":"548","DOI":"10.1016\/j.bbrc.2010.01.061","article-title":"Examination of the MASH1 gene in patients with Parkinson's disease","volume":"392","author":"Deng","year":"2010","journal-title":"Biochemical and Biophysical Research Communications"},{"key":"10.1016\/j.neulet.2012.03.097_bib0045","doi-asserted-by":"crossref","first-page":"1901","DOI":"10.1056\/NEJMoa0907006","article-title":"l-Histidine decarboxylase and Tourette's syndrome","volume":"362","author":"Ercan-Sencicek","year":"2010","journal-title":"The New England Journal of Medicine"},{"key":"10.1016\/j.neulet.2012.03.097_bib0050","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1016\/j.neulet.2011.05.245","article-title":"HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease","volume":"501","author":"Guo","year":"2011","journal-title":"Neuroscience Letters"},{"key":"10.1016\/j.neulet.2012.03.097_bib0055","doi-asserted-by":"crossref","first-page":"1184","DOI":"10.1056\/NEJMra010032","article-title":"Tourette's syndrome","volume":"345","author":"Jankovic","year":"2001","journal-title":"The New England Journal of Medicine"},{"key":"10.1016\/j.neulet.2012.03.097_bib0060","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1016\/j.pediatrneurol.2007.02.015","article-title":"Candidate locus for chorea and tic disorders at 15q?","volume":"37","author":"Jankovic","year":"2007","journal-title":"Pediatric Neurology"},{"key":"10.1016\/j.neulet.2012.03.097_bib0065","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1002\/(SICI)1096-8628(20000207)96:1<69::AID-AJMG14>3.0.CO;2-5","article-title":"Peek-a-boo fragile site at 16d associated with Tourette syndrome bipolar disorder, autistic disorder, and mental retardation","volume":"96","author":"Kerbeshian","year":"2000","journal-title":"American Journal of Medical Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0070","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1002\/1096-8628(20010701)101:3<259::AID-AJMG1374>3.0.CO;2-#","article-title":"Candidate region for Gilles de la Tourette syndrome at 7q31","volume":"101","author":"Kroisel","year":"2001","journal-title":"American Journal of Medical Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0075","doi-asserted-by":"crossref","first-page":"614","DOI":"10.1038\/sj.ejhg.5202006","article-title":"Familial deletion within NLGN4 associated with autism and Tourette syndrome","volume":"16","author":"Lawson-Yuen","year":"2008","journal-title":"European Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0080","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1002\/ajmg.b.32003","article-title":"Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome","volume":"159B","author":"Lei","year":"2012","journal-title":"American Journal of Medical Genetics Part B: Neuropsychiatric Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0085","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1086\/424389","article-title":"Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region","volume":"75","author":"Paschou","year":"2004","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0090","doi-asserted-by":"crossref","first-page":"634","DOI":"10.1038\/ejhg.2010.238","article-title":"Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome","volume":"19","author":"Patel","year":"2011","journal-title":"European Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0095","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1007\/s00438-006-0173-1","article-title":"Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome","volume":"277","author":"Petek","year":"2007","journal-title":"Molecular Genetics and Genomics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0100","doi-asserted-by":"crossref","first-page":"848","DOI":"10.1086\/319523","article-title":"Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome","volume":"68","author":"Petek","year":"2001","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0105","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1016\/j.jpsychores.2006.06.011","article-title":"A patient with both Gilles de la Tourette's syndrome and chromosome 22q11 deletion syndrome: clue to the genetics of Gilles de la Tourette's syndrome?","volume":"61","author":"Robertson","year":"2006","journal-title":"Journal of Psychosomatic Research"},{"key":"10.1016\/j.neulet.2012.03.097_bib0110","doi-asserted-by":"crossref","first-page":"620","DOI":"10.1111\/j.1365-2788.2006.00943.x","article-title":"An individual with Gilles de la Tourette syndrome and Smith\u2013Magenis microdeletion syndrome: is chromosome 17p11.2 a candidate region for Tourette syndrome putative susceptibility genes?","volume":"51","author":"Shelley","year":"2007","journal-title":"Journal of Intellectual Disability Research"},{"key":"10.1016\/j.neulet.2012.03.097_bib0115","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1002\/ajmg.1192","article-title":"Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners","volume":"105","author":"Simonic","year":"2001","journal-title":"American Journal of Medical Genetics"},{"key":"10.1016\/j.neulet.2012.03.097_bib0120","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1002\/ana.22398","article-title":"Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder","volume":"69","author":"Sundaram","year":"2011","journal-title":"Annals of Neurology"},{"key":"10.1016\/j.neulet.2012.03.097_bib0125","doi-asserted-by":"crossref","first-page":"1013","DOI":"10.1001\/archneur.1993.00540100012008","article-title":"Definitions and classification of tic disorders","volume":"50","year":"1993","journal-title":"Archives of Neurology"},{"key":"10.1016\/j.neulet.2012.03.097_bib0130","doi-asserted-by":"crossref","first-page":"954","DOI":"10.1038\/sj.mp.4001877","article-title":"Genetic clinical analysis of a large Dutch Gilles de la Tourette family","volume":"11","author":"Verkerk","year":"2006","journal-title":"Molecular Psychiatry"},{"key":"10.1016\/j.neulet.2012.03.097_bib0135","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/S0888-7543(03)00097-1","article-title":"CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder","volume":"82","author":"Verkerk","year":"2003","journal-title":"Genomics"}],"container-title":["Neuroscience Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394012005101?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394012005101?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,6,26]],"date-time":"2019-06-26T23:00:50Z","timestamp":1561590050000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0304394012005101"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,5]]},"references-count":27,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2012,5]]}},"alternative-id":["S0304394012005101"],"URL":"https:\/\/doi.org\/10.1016\/j.neulet.2012.03.097","relation":{},"ISSN":["0304-3940"],"issn-type":[{"value":"0304-3940","type":"print"}],"subject":[],"published":{"date-parts":[[2012,5]]}}}