{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T02:53:46Z","timestamp":1761101626649},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2000,3,22]]},"DOI":"10.1093\/hmg\/9.5.735","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T22:22:25Z","timestamp":1027722145000},"page":"735-744","source":"Crossref","is-referenced-by-count":74,"title":["Batten disease: evaluation of CLN3 mutations on protein localization and function"],"prefix":"10.1093","volume":"9","author":[{"given":"R. E.","family":"Haskell","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","container-title":["Human Molecular Genetics"],"original-title":[],"link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/9\/5\/735\/9815152\/090735.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,24]],"date-time":"2017-08-24T10:45:53Z","timestamp":1503571553000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/9.5.735"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,3,22]]},"references-count":0,"journal-issue":{"issue":"5"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/9.5.735","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,3,22]]}}}