{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,20]],"date-time":"2026-09-20T22:15:32Z","timestamp":1789942532312,"version":"4.0.1"},"reference-count":10,"publisher":"Oxford University Press (OUP)","issue":"6","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":178,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clin Exp Dermatol"],"published-print":{"date-parts":[[2015,8]]},"DOI":"10.1111\/ced.12616","type":"journal-article","created":{"date-parts":[[2015,3,7]],"date-time":"2015-03-07T06:25:06Z","timestamp":1425709506000},"page":"636-639","source":"Crossref","is-referenced-by-count":9,"title":["Infantile systemic hyalinosis in an Iranian family with a mutation in the<i>CMG2\/ANTXR2<\/i>gene"],"prefix":"10.1093","volume":"40","author":[{"given":"H.","family":"Vahidnezhad","sequence":"first","affiliation":[{"name":"Biotechnology Research Center; Department of Molecular Medicine; Pasteur Institute of Iran; Tehran Iran"},{"name":"Department of Medical Genetics; School of Medicine; Tehran University of Medical Sciences; Tehran Iran"},{"name":"Department of Dermatology and Cutaneous Biology; Thomas Jefferson University; Philadelphia Pennsylvania USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"V.","family":"Ziaee","sequence":"additional","affiliation":[{"name":"Pediatric Rheumatology Research Group, Rheumatology Research Center; Tehran University of Medical Sciences; Tehran Iran"},{"name":"Department of Pediatrics, Children's Medical Center; Pediatrics Center of Excellence, Tehran University of Medical Sciences; Tehran Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L.","family":"Youssefian","sequence":"additional","affiliation":[{"name":"Department of Medical Genetics; School of Medicine; Tehran University of Medical Sciences; Tehran Iran"},{"name":"Department of Dermatology and Cutaneous Biology; Thomas Jefferson University; Philadelphia Pennsylvania USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Q.","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Dermatology and Cutaneous Biology; Thomas Jefferson University; Philadelphia Pennsylvania USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Sotoudeh","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Children's Medical Center; Pediatric Center of Excellence; Tehran University of Medical Sciences; Tehran Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.","family":"Uitto","sequence":"additional","affiliation":[{"name":"Department of Dermatology and Cutaneous Biology; Thomas Jefferson University; Philadelphia Pennsylvania USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2015,3,7]]},"reference":[{"key":"10.1111\/ced.12616-BIB0001|ced12616-cit-0001","doi-asserted-by":"crossref","first-page":"e1485","DOI":"10.1542\/peds.2006-0824","article-title":"Systemic hyalinosis: a distinctive early childhood-onset disorder characterized by mutations in the anthrax toxin receptor 2 gene (ANTRX2)","volume":"118","author":"Shieh","year":"2006","journal-title":"Pediatrics"},{"key":"10.1111\/ced.12616-BIB0002|ced12616-cit-0002","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1007\/s10067-005-0124-y","article-title":"Infantile systemic hyalinosis: report of three Iranian children and review of the literature","volume":"26","author":"Aghighi","year":"2007","journal-title":"Clin Rheumatol"},{"key":"10.1111\/ced.12616-BIB0003|ced12616-cit-0003","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1038\/emboj.2011.442","article-title":"The dark sides of capillary morphogenesis gene 2","volume":"31","author":"Deuquet","year":"2012","journal-title":"EMBO J"},{"key":"10.1111\/ced.12616-BIB0004|ced12616-cit-0004","doi-asserted-by":"crossref","first-page":"791","DOI":"10.1086\/378418","article-title":"Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis","volume":"73","author":"Hanks","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1111\/ced.12616-BIB0005|ced12616-cit-0005","doi-asserted-by":"crossref","first-page":"5170","DOI":"10.1073\/pnas.0431098100","article-title":"Human capillary morphogenesis protein 2 functions as an anthrax toxin receptor","volume":"100","author":"Scobie","year":"2003","journal-title":"Proc Natl Acad Sci USA"},{"key":"10.1111\/ced.12616-BIB0006|ced12616-cit-0006","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1111\/j.1365-2133.2010.09769.x","article-title":"Spectrum of mutations in the ANTXR2 (CMG2) gene in infantile systemic hyalinosis and juvenile hyaline fibromatosis","volume":"163","author":"El-Kamah","year":"2010","journal-title":"Br J Dermatol"},{"key":"10.1111\/ced.12616-BIB0007|ced12616-cit-0007","doi-asserted-by":"crossref","first-page":"732","DOI":"10.1002\/ajmg.a.35228","article-title":"Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system","volume":"158A","author":"Denadai","year":"2012","journal-title":"Am J Med Genet A"},{"key":"10.1111\/ced.12616-BIB0008|ced12616-cit-0008","doi-asserted-by":"crossref","first-page":"1005","DOI":"10.1002\/humu.22324","article-title":"In-depth analysis of hyaline fibromatosis syndrome frameshift mutations at the same site reveal the necessity of personalized therapy","volume":"34","author":"Yan","year":"2013","journal-title":"Hum Mutat"},{"key":"10.1111\/ced.12616-BIB0009|ced12616-cit-0009","doi-asserted-by":"crossref","first-page":"695","DOI":"10.1016\/j.jaad.2009.01.039","article-title":"Juvenile hyaline fibromatosis and infantile systemic hyalinosis: a unifying term and a proposed grading system","volume":"61","author":"Nofal","year":"2009","journal-title":"J Am Acad Dermatol"},{"key":"10.1111\/ced.12616-BIB0010|ced12616-cit-0010","doi-asserted-by":"crossref","first-page":"2755","DOI":"10.1242\/jcs.114.15.2755","article-title":"Differential gene expression during capillary morphogenesis in 3D collagen matrices: regulated expression of genes involved in basement membrane matrix assembly, cell cycle progression, cellular differentiation and G-protein signaling","volume":"114","author":"Bell","year":"2001","journal-title":"J Cell Sci"}],"container-title":["Clinical and Experimental Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fced.12616","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/ced.12616\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,2,14]],"date-time":"2023-02-14T14:41:11Z","timestamp":1676385671000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/ced\/article\/40\/6\/636\/6621376"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,3,7]]},"references-count":10,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2015,8]]}},"URL":"https:\/\/doi.org\/10.1111\/ced.12616","relation":{},"ISSN":["0307-6938"],"issn-type":[{"value":"0307-6938","type":"print"}],"subject":[],"published":{"date-parts":[[2015,3,7]]}}}