{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T13:18:33Z","timestamp":1791206313491,"version":"4.1.0"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"16","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Human Molecular Genetics"],"DOI":"10.1093\/hmg\/ddh192","type":"journal-article","created":{"date-parts":[[2004,7,1]],"date-time":"2004-07-01T01:46:00Z","timestamp":1088646360000},"page":"1763-1773","source":"Crossref","is-referenced-by-count":145,"title":["Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-\u00a0B activation"],"prefix":"10.1093","volume":"13","author":[{"given":"F.","family":"Fusco","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2004,6,15]]},"container-title":["Human Molecular Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/13\/16\/1763\/1960509\/ddh192.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T04:37:10Z","timestamp":1503463030000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/ddh192"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,6,15]]},"references-count":0,"journal-issue":{"issue":"16","published-online":{"date-parts":[[2004,6,15]]}},"URL":"https:\/\/doi.org\/10.1093\/hmg\/ddh192","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[2004,6,15]]}}}