{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T04:55:26Z","timestamp":1790744126641,"version":"4.1.0"},"reference-count":13,"publisher":"Elsevier BV","issue":"11","license":[{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2018,11,1]],"date-time":"2018-11-01T00:00:00Z","timestamp":1541030400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie"],"published-print":{"date-parts":[[2018,11]]},"DOI":"10.1016\/j.annder.2018.07.014","type":"journal-article","created":{"date-parts":[[2018,9,11]],"date-time":"2018-09-11T19:52:33Z","timestamp":1536695553000},"page":"683-689","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":6,"title":["Lupus-engelures familial\u00a0: quatre cas sur trois g\u00e9n\u00e9rations"],"prefix":"10.1016","volume":"145","author":[{"given":"A.-S.","family":"Beltoise","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C.","family":"Audouin-Pajot","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P.","family":"Lucas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"Tournier","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G.-I.","family":"Rice","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y.-J.","family":"Crow","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.","family":"Mazereeuw-Hautier","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.annder.2018.07.014_bib0070","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1111\/j.1749-6632.2011.06220.x","article-title":"Type I interferonopathies: a novel set of inborn errors of immunity: Type I interferonopathies","volume":"1238","author":"Crow","year":"2011","journal-title":"Annals N Y Acad Sci"},{"key":"10.1016\/j.annder.2018.07.014_bib0075","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1016\/j.revmed.2016.08.016","article-title":"Les interf\u00e9ronopathies de type I. Mise au point et revue de la litt\u00e9rature","volume":"39","author":"Picard","year":"2018","journal-title":"Rev Med Interne"},{"key":"10.1016\/j.annder.2018.07.014_bib0080","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/j.jaad.2013.04.020","article-title":"Systemic involvement in TREX1-associated familial chilblain lupus","volume":"69","author":"G\u00fcnther","year":"2013","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.annder.2018.07.014_bib0085","doi-asserted-by":"crossref","first-page":"653","DOI":"10.1016\/j.annder.2015.06.018","article-title":"Interf\u00e9ronopathies de type 1","volume":"142","author":"Munoz","year":"2015","journal-title":"Ann Dermatol Venereol"},{"key":"10.1016\/j.annder.2018.07.014_bib0090","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1002\/ajmg.a.36887","article-title":"Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1","volume":"167","author":"Crow","year":"2015","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.annder.2018.07.014_bib0095","doi-asserted-by":"crossref","first-page":"713","DOI":"10.1086\/521373","article-title":"Clinical and Molecular Phenotype of Aicardi-Gouti\u00e8res Syndrome","volume":"81","author":"Rice","year":"2007","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2018.07.014_bib0100","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1007\/s10875-015-0147-3","article-title":"Human Disease Phenotypes Associated With Mutations in TREX1","volume":"35","author":"Rice","year":"2015","journal-title":"J Clin Immunol"},{"key":"10.1016\/j.annder.2018.07.014_bib0105","doi-asserted-by":"crossref","first-page":"811","DOI":"10.1086\/513443","article-title":"Heterozygous Mutations in TREX1\u00a0Cause Familial Chilblain Lupus and Dominant Aicardi-Gouti\u00e8res Syndrome","volume":"80","author":"Rice","year":"2007","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2018.07.014_bib0110","doi-asserted-by":"crossref","first-page":"811","DOI":"10.1086\/513443","article-title":"Heterozygous Mutations in TREX1\u00a0Cause Familial Chilblain Lupus and Dominant Aicardi-Gouti\u00e8res Syndrome","volume":"80","author":"Rice","year":"2007","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2018.07.014_bib0115","doi-asserted-by":"crossref","first-page":"731","DOI":"10.1086\/507848","article-title":"Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p","volume":"79","author":"Lee-Kirsch","year":"2006","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2018.07.014_bib0120","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1111\/j.1365-2133.2012.10813.x","article-title":"Inherited or de novo mutation affecting aspartate 18\u00a0of TREX1\u00a0results in either familial chilblain lupus or Aicardi-Gouti\u00e8res syndrome","volume":"167","author":"T\u00fcngler","year":"2012","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2018.07.014_bib0125","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1186\/1742-4690-8-91","article-title":"An autoimmune disease prevented by anti-retroviral drugs","volume":"8","author":"Beck-Engeser","year":"2011","journal-title":"Retrovirology"},{"key":"10.1016\/j.annder.2018.07.014_bib0130","doi-asserted-by":"crossref","first-page":"2081","DOI":"10.1002\/art.40179","article-title":"Musculoskeletal Disease in MDA5-Related Type I Interferonopathy: A Mendelian Mimic of Jaccoud's Arthropathy","volume":"69","author":"de Carvalho","year":"2017","journal-title":"Arthritis Rheum"}],"container-title":["Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0151963818305052?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0151963818305052?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T11:06:20Z","timestamp":1758971180000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0151963818305052"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,11]]},"references-count":13,"journal-issue":{"issue":"11","published-print":{"date-parts":[[2018,11]]}},"alternative-id":["S0151963818305052"],"URL":"https:\/\/doi.org\/10.1016\/j.annder.2018.07.014","relation":{},"ISSN":["0151-9638"],"issn-type":[{"value":"0151-9638","type":"print"}],"subject":[],"published":{"date-parts":[[2018,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Lupus-engelures familial\u00a0: quatre cas sur trois g\u00e9n\u00e9rations","name":"articletitle","label":"Article Title"},{"value":"Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.annder.2018.07.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}