{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T12:25:45Z","timestamp":1791116745434,"version":"4.1.0"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1998,2,1]]},"DOI":"10.1093\/hmg\/7.2.165","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T18:20:49Z","timestamp":1027707649000},"page":"165-170","source":"Crossref","is-referenced-by-count":216,"title":["Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)"],"prefix":"10.1093","volume":"7","author":[{"given":"G","family":"David","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","container-title":["Human Molecular Genetics"],"original-title":[],"link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/7\/2\/165\/1795894\/7-2-165.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T01:57:33Z","timestamp":1503453453000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/7.2.165"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1998,2,1]]},"references-count":0,"journal-issue":{"issue":"2"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/7.2.165","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[1998,2,1]]}}}