{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,3]],"date-time":"2026-03-03T04:18:05Z","timestamp":1772511485697,"version":"3.50.1"},"reference-count":33,"publisher":"Elsevier BV","issue":"1-2","license":[{"start":{"date-parts":[[2006,9,1]],"date-time":"2006-09-01T00:00:00Z","timestamp":1157068800000},"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":[[2006,9]]},"DOI":"10.1016\/j.neulet.2006.06.038","type":"journal-article","created":{"date-parts":[[2006,7,30]],"date-time":"2006-07-30T02:01:00Z","timestamp":1154224860000},"page":"126-131","source":"Crossref","is-referenced-by-count":12,"title":["Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy"],"prefix":"10.1016","volume":"405","author":[{"given":"Toshimitsu","family":"Suzuki","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antonio V.","family":"Delgado-Escueta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria E.","family":"Alonso","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ryoji","family":"Morita","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nami","family":"Okamura","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshihisa","family":"Sugimoto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dongsheng","family":"Bai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marco T.","family":"Medina","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julia N.","family":"Bailey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Astrid","family":"Rasmussen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jaime","family":"Ramos-Peek","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sergio","family":"Cordova","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francisco","family":"Rubio-Donnadieu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Adriana","family":"Ochoa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aurelio","family":"Jara-Prado","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Johji","family":"Inazawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kazuhiro","family":"Yamakawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.neulet.2006.06.038_bib1","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1111\/j.1528-1157.1984.tb04163.x","article-title":"Some clinical and EEG aspects of benign juvenile myoclonic epilepsy","volume":"25","author":"Asconape","year":"1984","journal-title":"Epilepsia"},{"key":"10.1016\/j.neulet.2006.06.038_bib2","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1002\/ajmg.10724","article-title":"Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families","volume":"113","author":"Bai","year":"2002","journal-title":"Am. J. Med. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib3","first-page":"72","article-title":"Molecular genetic analysis of juvenile myoclonic epilepsy in the Saudi Arabian population","volume":"41","author":"Bata","year":"2000","journal-title":"Epilepsia"},{"key":"10.1016\/j.neulet.2006.06.038_bib4","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1002\/ana.410430405","article-title":"Epilepsies in twins: genetics of the major epilepsy syndromes","volume":"43","author":"Berkovic","year":"1998","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.neulet.2006.06.038_bib5","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1038\/ng885","article-title":"Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy","volume":"31","author":"Cossette","year":"2002","journal-title":"Nat. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib6","first-page":"82","article-title":"Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances","volume":"35","author":"Delgado-Escueta","year":"2002","journal-title":"Rev. Neurol."},{"key":"10.1016\/j.neulet.2006.06.038_bib7","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1212\/WNL.34.3.285","article-title":"Juvenile myoclonic epilepsy of Janz","volume":"34","author":"Delgado-Escueta","year":"1984","journal-title":"Neurology"},{"key":"10.1016\/j.neulet.2006.06.038_bib8","doi-asserted-by":"crossref","first-page":"1651","DOI":"10.1212\/WNL.41.10.1651","article-title":"Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients","volume":"41","author":"Durner","year":"1991","journal-title":"Neurology"},{"key":"10.1016\/j.neulet.2006.06.038_bib9","doi-asserted-by":"crossref","first-page":"1329","DOI":"10.1093\/hmg\/6.8.1329","article-title":"Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q","volume":"6","author":"Elmslie","year":"1997","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib10","doi-asserted-by":"crossref","first-page":"1531","DOI":"10.1086\/302909","article-title":"Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia","volume":"66","author":"Escayg","year":"2000","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib11","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1002\/ajmg.1320310125","article-title":"Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6","volume":"31","author":"Greenberg","year":"1988","journal-title":"Am. J. Med. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib12","doi-asserted-by":"crossref","first-page":"508","DOI":"10.1086\/302763","article-title":"Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy","volume":"66","author":"Greenberg","year":"2000","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib13","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1038\/ng1121","article-title":"Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies","volume":"33","author":"Haug","year":"2003","journal-title":"Nat. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib14","series-title":"Epilepsy: Frequency, Causes and Consequences","author":"Hauser","year":"1990"},{"key":"10.1016\/j.neulet.2006.06.038_bib15","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1159\/000133618","article-title":"High resolution ordering of DNA markers by multi-color fluorescent in situ hybridization of prophase chromosomes","volume":"65","author":"Inazawa","year":"1994","journal-title":"Cytogenet. Cell Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib16","first-page":"372","article-title":"Therapy of matutinal epilepsy","volume":"45","author":"Janz","year":"1969","journal-title":"Z. Allgemeinmed."},{"key":"10.1016\/j.neulet.2006.06.038_bib17","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1093\/nar\/gkg129","article-title":"The UCSC Genome Browser Database","volume":"31","author":"Karolchik","year":"2003","journal-title":"Nucleic Acids Res."},{"key":"10.1016\/j.neulet.2006.06.038_bib18","doi-asserted-by":"crossref","first-page":"4430","DOI":"10.4049\/jimmunol.167.8.4430","article-title":"Identification of a novel cytokine, ML-1, and its expression in subjects with asthma","volume":"167","author":"Kawaguchi","year":"2001","journal-title":"J. Immunol."},{"key":"10.1016\/j.neulet.2006.06.038_bib19","doi-asserted-by":"crossref","first-page":"656","DOI":"10.1101\/gr.229202. Article published online before March 2002","article-title":"BLAT\u2014the BLAST-like alignment tool","volume":"12","author":"Kent","year":"2002","journal-title":"Genome Res."},{"key":"10.1016\/j.neulet.2006.06.038_bib20","doi-asserted-by":"crossref","first-page":"996","DOI":"10.1101\/gr.229102. Article published online before print in May 2002","article-title":"The human genome browser at UCSC","volume":"12","author":"Kent","year":"2002","journal-title":"Genome Res."},{"key":"10.1016\/j.neulet.2006.06.038_bib21","doi-asserted-by":"crossref","first-page":"438","DOI":"10.1002\/(SICI)1096-8628(19960614)63:3<438::AID-AJMG5>3.0.CO;2-N","article-title":"Juvenile myoclonic epilepsy in chromosome 6p12-p11: locus heterogeneity and recombinations","volume":"63","author":"Liu","year":"1996","journal-title":"Am. J. Med. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib22","first-page":"368","article-title":"Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: linkage to convulsions and electroencephalography trait","volume":"57","author":"Liu","year":"1995","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib23","first-page":"223","article-title":"Genetics of myoclonic and myoclonus epilepsies","volume":"3","author":"Minassian","year":"1995","journal-title":"Clin. Neurosci."},{"key":"10.1016\/j.neulet.2006.06.038_bib24","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1016\/S0920-1211(99)00061-3","article-title":"Exclusion of the JRK\/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24","volume":"37","author":"Morita","year":"1999","journal-title":"Epilepsy Res."},{"key":"10.1016\/j.neulet.2006.06.038_bib25","doi-asserted-by":"crossref","first-page":"2064","DOI":"10.1212\/WNL.53.9.2064","article-title":"Prevalence of epilepsy in rural Bolivia: a door-to-door survey","volume":"53","author":"Nicoletti","year":"1999","journal-title":"Neurology"},{"key":"10.1016\/j.neulet.2006.06.038_bib26","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1111\/j.1528-1157.1994.tb02432.x","article-title":"Juvenile myoclonic epilepsy: a 5-year prospective study","volume":"35","author":"Panayiotopoulos","year":"1994","journal-title":"Epilepsia"},{"key":"10.1016\/j.neulet.2006.06.038_bib27","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1093\/hmg\/ddi018","article-title":"Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13","volume":"14","author":"Pinto","year":"2005","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib28","doi-asserted-by":"crossref","first-page":"449","DOI":"10.1002\/ana.20598","article-title":"A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26","volume":"58","author":"Puranam","year":"2005","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.neulet.2006.06.038_bib29","doi-asserted-by":"crossref","first-page":"264","DOI":"10.1006\/geno.2000.6296","article-title":"Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map","volume":"68","author":"Sugimoto","year":"2000","journal-title":"Genomics"},{"key":"10.1016\/j.neulet.2006.06.038_bib30","doi-asserted-by":"crossref","first-page":"842","DOI":"10.1038\/ng1393","article-title":"Mutations in EFHC1 cause juvenile myoclonic epilepsy","volume":"36","author":"Suzuki","year":"2004","journal-title":"Nat. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib31","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1016\/S0920-1211(02)00052-9","article-title":"Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5","volume":"50","author":"Suzuki","year":"2002","journal-title":"Epilepsy Res."},{"key":"10.1016\/j.neulet.2006.06.038_bib32","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1038\/ng833","article-title":"The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein","volume":"30","author":"Ward","year":"2002","journal-title":"Nat. Genet."},{"key":"10.1016\/j.neulet.2006.06.038_bib33","doi-asserted-by":"crossref","first-page":"1201","DOI":"10.1093\/hmg\/4.7.1201","article-title":"Mapping of genes predisposing to idiopathic generalized epilepsy","volume":"4","author":"Zara","year":"1995","journal-title":"Hum. Mol. Genet."}],"container-title":["Neuroscience Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394006006288?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394006006288?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,1,14]],"date-time":"2019-01-14T13:52:30Z","timestamp":1547473950000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0304394006006288"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2006,9]]},"references-count":33,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2006,9]]}},"alternative-id":["S0304394006006288"],"URL":"https:\/\/doi.org\/10.1016\/j.neulet.2006.06.038","relation":{},"ISSN":["0304-3940"],"issn-type":[{"value":"0304-3940","type":"print"}],"subject":[],"published":{"date-parts":[[2006,9]]}}}