{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,19]],"date-time":"2026-01-19T10:38:12Z","timestamp":1768819092550,"version":"3.49.0"},"reference-count":11,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[1999,4,1]],"date-time":"1999-04-01T00:00:00Z","timestamp":922924800000},"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":["Molecular Genetics and Metabolism"],"published-print":{"date-parts":[[1999,4]]},"DOI":"10.1006\/mgme.1999.2835","type":"journal-article","created":{"date-parts":[[2002,10,7]],"date-time":"2002-10-07T14:37:46Z","timestamp":1034001466000},"page":"344-348","source":"Crossref","is-referenced-by-count":9,"title":["Clinical and Molecular Analysis of Japanese Patients with Neuronal Ceroid Lipofuscinosis"],"prefix":"10.1006","volume":"66","author":[{"given":"Kimihiko","family":"Oishi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroyuki","family":"Ida","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenji","family":"Kurosawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshikatsu","family":"Eto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1006\/mgme.1999.2835_RF1","doi-asserted-by":"crossref","first-page":"80","DOI":"10.1016\/S0387-7604(88)80075-5","article-title":"Neuronal ceroid lipofuscinosis in childhood","volume":"10","author":"Santavuori","year":"1989","journal-title":"Brain Dev"},{"key":"10.1006\/mgme.1999.2835_RF2","doi-asserted-by":"crossref","first-page":"150","DOI":"10.1002\/ajmg.1320570208","article-title":"Classification of the neuronal ceroid lipofuscinosis","volume":"57","author":"Dyken","year":"1995","journal-title":"Am J Med Genet"},{"key":"10.1006\/mgme.1999.2835_RF3","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1055\/s-2007-973654","article-title":"Neuronal ceroid lipofuscinosis in Scandinavia: Epidemiology and clinical pictures","volume":"28","author":"Uvebrant","year":"1997","journal-title":"Neuropediatrics"},{"key":"10.1006\/mgme.1999.2835_RF4","doi-asserted-by":"crossref","first-page":"525","DOI":"10.1002\/ajmg.1320420420","article-title":"Variability in the clinical and pathological findings in the neuronal ceroid lipofuscinosis: Review of data and observations","volume":"42","author":"Wisniewski","year":"1992","journal-title":"Am J Med Genet"},{"key":"10.1006\/mgme.1999.2835_RF5","doi-asserted-by":"crossref","first-page":"144","DOI":"10.1002\/ajmg.1320570207","article-title":"Childhood neuronal ceroid-lipofuscinoses in Argentina","volume":"57","author":"Taratuto","year":"1995","journal-title":"Am J Med Genet"},{"key":"10.1006\/mgme.1999.2835_RF6","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1002\/ajmg.1320570206","article-title":"Neuronal ceroid-lipofuscinoses in Italy: An epidemiological study","volume":"57","author":"Cardona","year":"1995","journal-title":"Am J Med Genet"},{"key":"10.1006\/mgme.1999.2835_RF7","doi-asserted-by":"crossref","first-page":"536","DOI":"10.1002\/ajmg.1320420422","article-title":"Incidence of neuronal ceroid-lipofuscinoses in West Germany: Variation of a method for studying autosomal recessive disorders","volume":"42","author":"Claussen","year":"1992","journal-title":"Am J Med Genet"},{"key":"10.1006\/mgme.1999.2835_RF8","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1016\/0092-8674(95)90274-0","volume":"82","year":"1995","journal-title":"Cell"},{"key":"10.1006\/mgme.1999.2835_RF9","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1086\/514846","article-title":"Spectrum of mutations in the Batten disease gene, CLN3","volume":"61","author":"Munroe","year":"1997","journal-title":"Am J Hum Genet"},{"key":"10.1006\/mgme.1999.2835_RF10","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1136\/jmg.34.11.955","article-title":"Rapid detection of the major deletion in the Batten disease gene CLN3 by allele specific PCR","volume":"34","author":"Taschner","year":"1997","journal-title":"J Med Genet"},{"key":"10.1006\/mgme.1999.2835_RF11","doi-asserted-by":"crossref","first-page":"1014","DOI":"10.1016\/S0140-6736(96)90148-8","article-title":"Prenatal diagnosis of Batten's disease","volume":"347","author":"Munroe","year":"1996","journal-title":"Lancet"}],"container-title":["Molecular Genetics and Metabolism"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1096719299928354?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1096719299928354?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,5,7]],"date-time":"2019-05-07T20:20:54Z","timestamp":1557260454000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1096719299928354"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1999,4]]},"references-count":11,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1999,4]]}},"alternative-id":["S1096719299928354"],"URL":"https:\/\/doi.org\/10.1006\/mgme.1999.2835","relation":{},"ISSN":["1096-7192"],"issn-type":[{"value":"1096-7192","type":"print"}],"subject":[],"published":{"date-parts":[[1999,4]]}}}