{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T18:15:40Z","timestamp":1791137740344,"version":"4.1.0"},"reference-count":62,"publisher":"Elsevier BV","issue":"6-7","license":[{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"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":[[2008,6]]},"DOI":"10.1016\/j.annder.2008.04.006","type":"journal-article","created":{"date-parts":[[2008,6,5]],"date-time":"2008-06-05T08:19:33Z","timestamp":1212653973000},"page":"466-478","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"title":["Syndromes avec vieillissement cutan\u00e9 pr\u00e9matur\u00e9\u00a0: de l\u2019expression ph\u00e9notypique au g\u00e8ne"],"prefix":"10.1016","volume":"135","author":[{"given":"O.","family":"Dereure","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"Marque","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B.","family":"Guillot","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.annder.2008.04.006_bib1","doi-asserted-by":"crossref","first-page":"109","DOI":"10.1016\/S0733-8635(18)30769-1","article-title":"Syndromes of premature aging","volume":"5","author":"Beauregard","year":"1987","journal-title":"Dermatol Clin"},{"key":"10.1016\/j.annder.2008.04.006_bib2","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1016\/0738-081X(95)00151-5","article-title":"The premature aging syndromes","volume":"14","author":"Pesce","year":"1996","journal-title":"Clin Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib3","doi-asserted-by":"crossref","first-page":"947","DOI":"10.1016\/j.biocel.2004.10.011","article-title":"Genetic alterations in accelerated ageing syndromes. Do they play a role in natural ageing?","volume":"37","author":"Puzianowska-Kuznicka","year":"2005","journal-title":"Int J Biochem Cell Biol"},{"issue":"Spec No 2","key":"10.1016\/j.annder.2008.04.006_bib4","doi-asserted-by":"crossref","first-page":"R151","DOI":"10.1093\/hmg\/ddl214","article-title":"Molecular bases of progeroid syndromes","volume":"15","author":"Navarro","year":"2006","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib5","doi-asserted-by":"crossref","first-page":"2603","DOI":"10.1002\/ajmg.a.31346","article-title":"Hutchinson-Gilford progeria syndrome: review of the phenotype","volume":"140","author":"Hennekam","year":"2006","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.annder.2008.04.006_bib6","doi-asserted-by":"crossref","first-page":"1308","DOI":"10.1111\/j.1365-2133.2007.07897.x","article-title":"Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature","volume":"156","author":"Mazereeuw-Hautier","year":"2007","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib7","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1038\/nature01629","article-title":"Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome","volume":"423","author":"Eriksson","year":"2003","journal-title":"Nature"},{"key":"10.1016\/j.annder.2008.04.006_bib8","doi-asserted-by":"crossref","first-page":"2055","DOI":"10.1126\/science.1084125","article-title":"Lamin a truncation in Hutchinson-Gilford progeria","volume":"300","author":"De Sandre-Giovannoli","year":"2003","journal-title":"Science"},{"key":"10.1016\/j.annder.2008.04.006_bib9","doi-asserted-by":"crossref","first-page":"8963","DOI":"10.1073\/pnas.0402943101","article-title":"Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome","volume":"101","author":"Goldman","year":"2004","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.annder.2008.04.006_bib10","doi-asserted-by":"crossref","first-page":"e36","DOI":"10.1136\/jmg.2004.029751","article-title":"Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotype","volume":"42","author":"Shackleton","year":"2005","journal-title":"J Med Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib11","doi-asserted-by":"crossref","first-page":"524","DOI":"10.1002\/humu.20315","article-title":"A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPS","volume":"27","author":"Denecke","year":"2006","journal-title":"Hum Mutat"},{"key":"10.1016\/j.annder.2008.04.006_bib12","doi-asserted-by":"crossref","first-page":"882","DOI":"10.1002\/humu.20536","article-title":"Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes","volume":"28","author":"Moulson","year":"2007","journal-title":"Hum Mutat"},{"key":"10.1016\/j.annder.2008.04.006_bib13","doi-asserted-by":"crossref","first-page":"517","DOI":"10.1210\/jc.2005-1297","article-title":"A homozygous mutation in the lamin A\/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features","volume":"91","author":"Van Esch","year":"2006","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.annder.2008.04.006_bib14","doi-asserted-by":"crossref","first-page":"4467","DOI":"10.1210\/jc.2007-0116","article-title":"Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype","volume":"92","author":"Lombardi","year":"2007","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.annder.2008.04.006_bib15","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1111\/j.1365-2133.1980.tb06595.x","article-title":"Familial acrogeria (Gottron)","volume":"103","author":"de Groot","year":"1980","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib16","doi-asserted-by":"crossref","first-page":"178","DOI":"10.1046\/j.1365-2133.2000.03266.x","article-title":"COL3A1 mutation leading to acrogeria (Gottron Type)","volume":"142","author":"Jansen","year":"2000","journal-title":"Br J Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib17","first-page":"975","article-title":"Simultaneous occurrence of metageria and Gottron's acrogeria in one family","volume":"60","author":"Kaufmann","year":"1985","journal-title":"Z Hautkr"},{"key":"10.1016\/j.annder.2008.04.006_bib18","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1002\/ajmg.1320440313","article-title":"Acrometageria\u00a0: a spectrum of \u201cpremature aging\u201d syndromes","volume":"44","author":"Greally","year":"1992","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib19","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1111\/j.1600-0625.2007.00559.x","article-title":"Lessons learned from DNA repair defective syndromes","volume":"16","author":"Thoms","year":"2007","journal-title":"Exp Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib20","doi-asserted-by":"crossref","first-page":"253","DOI":"10.1021\/cr040483f","article-title":"Molecular mechanisms of mammalian global genome nucleotide excision repair","volume":"106","author":"Gillet","year":"2006","journal-title":"Chem Rev"},{"key":"10.1016\/j.annder.2008.04.006_bib21","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1002\/ajmg.1320420115","article-title":"Cockayne syndrome\u00a0: review of 140 cases","volume":"42","author":"Nance","year":"1992","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib22","doi-asserted-by":"crossref","first-page":"1442","DOI":"10.1212\/WNL.55.10.1442","article-title":"Cockayne syndrome and xeroderma pigmentosum","volume":"55","author":"Rapin","year":"2000","journal-title":"Neurology"},{"key":"10.1016\/j.annder.2008.04.006_bib23","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1016\/0092-8674(95)90028-4","article-title":"The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH","volume":"82","author":"Henning","year":"1995","journal-title":"Cell"},{"key":"10.1016\/j.annder.2008.04.006_bib24","doi-asserted-by":"crossref","first-page":"418","DOI":"10.1007\/BF02267059","article-title":"Genetic analysis of twenty-two patients with Cockayne syndrome","volume":"97","author":"Stefanini","year":"1996","journal-title":"Hum Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib25","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1086\/301686","article-title":"Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome","volume":"62","author":"Mallery","year":"1998","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib26","doi-asserted-by":"crossref","first-page":"564","DOI":"10.1038\/nrc1652","article-title":"Cancer in xeroderma pigmentosum and related disorders of DNA repair","volume":"5","author":"Cleaver","year":"2005","journal-title":"Nat Rev Cancer"},{"key":"10.1016\/j.annder.2008.04.006_bib27","doi-asserted-by":"crossref","first-page":"3116","DOI":"10.1073\/pnas.94.7.3116","article-title":"A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G\u00a0: implications for a second XPG function","volume":"94","author":"Nouspikel","year":"1997","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.annder.2008.04.006_bib28","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1097\/00005792-196605000-00001","article-title":"Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process","volume":"45","author":"Epstein","year":"1966","journal-title":"Medicine (Baltimore)"},{"key":"10.1016\/j.annder.2008.04.006_bib29","doi-asserted-by":"crossref","first-page":"1136","DOI":"10.1111\/j.1532-5415.1999.tb05240.x","article-title":"What geriatricians should know about the Werner syndrome","volume":"47","author":"Martin","year":"1999","journal-title":"J Am Geriatr Soc"},{"key":"10.1016\/j.annder.2008.04.006_bib30","first-page":"760","article-title":"Werner's syndrome\u00a0: from clinics to genetics","volume":"18","author":"Goto","year":"2000","journal-title":"Clin Exp Rheumatol"},{"key":"10.1016\/j.annder.2008.04.006_bib31","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1038\/ng0997-100","article-title":"The Werner syndrome protein is a DNA helicase","volume":"17","author":"Gray","year":"1997","journal-title":"Nat Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib32","first-page":"330","article-title":"Mutations in the consensus helicase domains of the Werner syndrome gene","volume":"60","author":"Yu","year":"1997","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib33","doi-asserted-by":"crossref","first-page":"440","DOI":"10.1016\/S0140-6736(03)14069-X","article-title":"LMNA mutations in atypical Werner's syndrome","volume":"362","author":"Chen","year":"2003","journal-title":"Lancet"},{"key":"10.1016\/j.annder.2008.04.006_bib34","doi-asserted-by":"crossref","first-page":"6699","DOI":"10.1210\/jc.2005-0939","article-title":"Phenotypic heterogeneity in body fat distribution in patients with atypical Werner's syndrome due to heterozygous Arg133Leu lamin A\/C mutation","volume":"90","author":"Jacob","year":"2005","journal-title":"J Clin Endocrinol Metab"},{"key":"10.1016\/j.annder.2008.04.006_bib35","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1016\/j.mrfmmm.2005.03.020","article-title":"Current advances in unraveling the function of the Werner syndrome protein","volume":"577","author":"Ozgenc","year":"2005","journal-title":"Mutat Res"},{"key":"10.1016\/j.annder.2008.04.006_bib36","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1016\/j.mad.2004.09.011","article-title":"Pathways and functions of the Werner syndrome protein","volume":"126","author":"Lee","year":"2005","journal-title":"Mech Ageing Dev"},{"key":"10.1016\/j.annder.2008.04.006_bib37","doi-asserted-by":"crossref","first-page":"954","DOI":"10.1038\/sj.onc.1205143","article-title":"Werner and Bloom helicases are involved in DNA repair in a complementary fashion","volume":"21","author":"Imamura","year":"2002","journal-title":"Oncogene"},{"key":"10.1016\/j.annder.2008.04.006_bib38","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1038\/sj.onc.1206906","article-title":"TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA","volume":"23","author":"Machwe","year":"2004","journal-title":"Oncogene"},{"key":"10.1016\/j.annder.2008.04.006_bib39","doi-asserted-by":"crossref","first-page":"1355","DOI":"10.1101\/gad.13.11.1355","article-title":"p53-mediated apoptosis is attenuated in Werner syndrome cells","volume":"13","author":"Spillare","year":"1999","journal-title":"Genes Dev"},{"key":"10.1016\/j.annder.2008.04.006_bib40","first-page":"95","article-title":"Bloom syndrome and ataxia telangiectasia","volume":"28","author":"Llerena","year":"1991","journal-title":"Semin Hematol"},{"key":"10.1016\/j.annder.2008.04.006_bib41","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/S0733-8635(18)30101-3","article-title":"Bloom's syndrome","volume":"13","author":"German","year":"1995","journal-title":"Dermatol Clin"},{"key":"10.1016\/j.annder.2008.04.006_bib42","doi-asserted-by":"crossref","first-page":"655","DOI":"10.1016\/0092-8674(95)90105-1","article-title":"The Bloom's syndrome gene product is homologous to RecQ helicases","volume":"83","author":"Ellis","year":"1995","journal-title":"Cell"},{"key":"10.1016\/j.annder.2008.04.006_bib43","first-page":"2766","article-title":"The BLM helicase is necessary for normal DNA double-strand break repair","volume":"62","author":"Langland","year":"2002","journal-title":"Cancer Res"},{"key":"10.1016\/j.annder.2008.04.006_bib44","doi-asserted-by":"crossref","first-page":"1210","DOI":"10.1093\/emboj\/cdg114","article-title":"BLM helicase-dependent transport of p53 to sites of stalled DNA replication forks modulates homologous recombination","volume":"22","author":"Sengupta","year":"2003","journal-title":"EMBO J"},{"key":"10.1016\/j.annder.2008.04.006_bib45","doi-asserted-by":"crossref","first-page":"1919","DOI":"10.1093\/hmg\/ddh193","article-title":"Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2","volume":"13","author":"Lillard-Wetherell","year":"2004","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib46","doi-asserted-by":"crossref","first-page":"750","DOI":"10.1016\/0190-9622(92)70249-F","article-title":"Rothmund-Thomson syndrome\u00a0: review of the world literature","volume":"27","author":"Vennos","year":"1992","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib47","doi-asserted-by":"crossref","first-page":"268","DOI":"10.1006\/geno.1999.5959","article-title":"Rothmund-Thomson syndrome responsible gene. RECQL4\u00a0: genomic structure and products","volume":"61","author":"Kitao","year":"1999","journal-title":"Genomics"},{"key":"10.1016\/j.annder.2008.04.006_bib48","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1111\/j.1749-6632.2001.tb05642.x","article-title":"Premature aging and predisposition to cancers caused by mutations in RecQ family helicases","volume":"928","author":"Furuichi","year":"2001","journal-title":"Ann N Y Acad Sci"},{"key":"10.1016\/j.annder.2008.04.006_bib49","doi-asserted-by":"crossref","first-page":"2421","DOI":"10.1093\/hmg\/ddh269","article-title":"RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway","volume":"13","author":"Yin","year":"2004","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib50","doi-asserted-by":"crossref","first-page":"2837","DOI":"10.1093\/hmg\/ddg306","article-title":"Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases","volume":"12","author":"Siitonen","year":"2003","journal-title":"Hum Mol Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib51","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1016\/S0190-9622(84)80089-4","article-title":"Common and uncommon cutaneous findings in patients with ataxia-telangiectasia","volume":"10","author":"Cohen","year":"1984","journal-title":"J Am Acad Dermatol"},{"key":"10.1016\/j.annder.2008.04.006_bib52","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1097\/00005792-199103000-00003","article-title":"Ataxia-telangiectasia\u00a0: an interdisciplinary approach to pathogenesis","volume":"70","author":"Gatti","year":"1991","journal-title":"Medicine (Baltimore)"},{"key":"10.1016\/j.annder.2008.04.006_bib53","first-page":"169","article-title":"Ataxia telangiectasia in the British Isles\u00a0: the clinical and laboratory features of 70 affected individuals","volume":"82","author":"Woods","year":"1992","journal-title":"Q J Med"},{"key":"10.1016\/j.annder.2008.04.006_bib54","doi-asserted-by":"crossref","first-page":"1831","DOI":"10.1056\/NEJM199112263252602","article-title":"Incidence of cancer in 161 families affected by ataxia-telangiectasia","volume":"325","author":"Swift","year":"1991","journal-title":"N Engl J Med"},{"key":"10.1016\/j.annder.2008.04.006_bib55","doi-asserted-by":"crossref","first-page":"125","DOI":"10.1002\/ajmg.10688","article-title":"Chromosome breakage syndromes and cancer","volume":"115","author":"Duker","year":"2002","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib56","doi-asserted-by":"crossref","first-page":"1009","DOI":"10.1136\/jcp.2005.026062","article-title":"Molecular pathology of ataxia telangiectasia","volume":"58","author":"Taylor","year":"2005","journal-title":"J Clin Pathol"},{"key":"10.1016\/j.annder.2008.04.006_bib57","doi-asserted-by":"crossref","first-page":"414","DOI":"10.4161\/cc.6.4.3886","article-title":"ATM and ATR\u00a0: components of an integrated circuit","volume":"6","author":"Hurley","year":"2007","journal-title":"Cell Cycle"},{"key":"10.1016\/j.annder.2008.04.006_bib58","first-page":"225","article-title":"Human syndromes with genomic instability and multiprotein machines that repair DNA double-strand breaks","volume":"18","author":"De la Torre","year":"2003","journal-title":"Histol Histopathol"},{"key":"10.1016\/j.annder.2008.04.006_bib59","first-page":"436","article-title":"Glycosaminoglycan-free small proteoglycan core protein is secreted by fibroblasts from a patient with a syndrome resembling progeroid","volume":"41","author":"Kresse","year":"1987","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib60","doi-asserted-by":"crossref","first-page":"1342","DOI":"10.1073\/pnas.87.4.1342","article-title":"A genetic defect in the biosynthesis of dermatan sulfate proteoglycan\u00a0: galactosyltransferase I deficiency in fibroblasts from a patient with a progeroid syndrome","volume":"87","author":"Quentin","year":"1990","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.annder.2008.04.006_bib61","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1007\/s10528-005-1068-2","article-title":"Defective glycosaminoglycan substitution of decorin in a patient with progeroid syndrome is a direct consequence of two point mutations in the galactosyltransferase I (beta4GalT-7) gene","volume":"43","author":"G\u00f6tte","year":"2005","journal-title":"Biochem Genet"},{"key":"10.1016\/j.annder.2008.04.006_bib62","doi-asserted-by":"crossref","first-page":"14416","DOI":"10.1073\/pnas.0503712102","article-title":"Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome","volume":"102","author":"Mallampalli","year":"2005","journal-title":"Proc Natl Acad Sci U S A"}],"container-title":["Annales de Dermatologie et de V\u00e9n\u00e9r\u00e9ologie"],"original-title":[],"language":"fr","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0151963808003591?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0151963808003591?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,27]],"date-time":"2025-09-27T10:54:04Z","timestamp":1758970444000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0151963808003591"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,6]]},"references-count":62,"journal-issue":{"issue":"6-7","published-print":{"date-parts":[[2008,6]]}},"alternative-id":["S0151963808003591"],"URL":"https:\/\/doi.org\/10.1016\/j.annder.2008.04.006","relation":{},"ISSN":["0151-9638"],"issn-type":[{"value":"0151-9638","type":"print"}],"subject":[],"published":{"date-parts":[[2008,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Syndromes avec vieillissement cutan\u00e9 pr\u00e9matur\u00e9\u00a0: de l\u2019expression ph\u00e9notypique au g\u00e8ne","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.2008.04.006","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2008 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}