{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,1]],"date-time":"2025-10-01T15:40:24Z","timestamp":1759333224078},"reference-count":10,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":532,"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":[[2014,4]]},"DOI":"10.1111\/ced.12293","type":"journal-article","created":{"date-parts":[[2014,3,18]],"date-time":"2014-03-18T06:44:40Z","timestamp":1395125080000},"page":"340-343","source":"Crossref","is-referenced-by-count":7,"title":["Kindler syndrome with severe mucosal involvement in childhood"],"prefix":"10.1093","volume":"39","author":[{"given":"C. V.","family":"Krishna","sequence":"first","affiliation":[{"name":"Department of Dermatology, Venereology and Leprology; Pondicherry Institute of Medical Sciences; Puducherry India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N. V.","family":"Parmar","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Venereology and Leprology; Pondicherry Institute of Medical Sciences; Puducherry India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Has","sequence":"additional","affiliation":[{"name":"Department of Dermatology; University Medical Center Freiburg; Freiburg Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2014,3,18]]},"reference":[{"key":"10.1111\/ced.12293-BIB0001|ced12293-cit-0001","doi-asserted-by":"crossref","first-page":"104","DOI":"10.1111\/j.1365-2133.1954.tb12598.x","article-title":"Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy","volume":"66","author":"Kindler","year":"1954","journal-title":"Br J Dermatol"},{"key":"10.1111\/ced.12293-BIB0002|ced12293-cit-0002","doi-asserted-by":"crossref","first-page":"961","DOI":"10.1902\/jop.2008.070167","article-title":"Kindler syndrome and periodontal disease: review of the literature and a 12-year follow-up case","volume":"79","author":"Wiebe","year":"2008","journal-title":"J Periodontol"},{"key":"10.1111\/ced.12293-BIB0003|ced12293-cit-0003","doi-asserted-by":"crossref","first-page":"336","DOI":"10.1016\/j.jaad.2005.06.030","article-title":"Cheilitis glandularis: a clinical marker for both malignancy and\/or severe inflammatory disease of the oral cavity","volume":"54","author":"Carrington","year":"2006","journal-title":"J Am Acad Dermatol"},{"key":"10.1111\/ced.12293-BIB0004|ced12293-cit-0004","doi-asserted-by":"crossref","first-page":"198","DOI":"10.2340\/00015555-0586","article-title":"Labial agglutination in a prepubertal girl: effect of topical oestrogen","volume":"89","author":"Velander","year":"2009","journal-title":"Acta Derm Venereol"},{"key":"10.1111\/ced.12293-BIB0005|ced12293-cit-0005","doi-asserted-by":"crossref","first-page":"563","DOI":"10.2340\/00015555-0314","article-title":"Novel and recurrent KIND1 mutations in two patients with KS and severe mucosal involvement","volume":"87","author":"Mansur","year":"2007","journal-title":"Acta Derm Venereol"},{"key":"10.1111\/ced.12293-BIB0006|ced12293-cit-0006","doi-asserted-by":"crossref","first-page":"209","DOI":"10.1016\/j.jdermsci.2008.07.007","article-title":"A novel large FERMT1 (KIND1) gene deletion in Kindler syndrome","volume":"52","author":"Has","year":"2008","journal-title":"J Dermatol Sci"},{"key":"10.1111\/ced.12293-BIB0007|ced12293-cit-0007","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1159\/000099328","article-title":"Pregnancy and delivery with Kindler syndrome","volume":"64","author":"Hayashi","year":"2007","journal-title":"Gynecol Obstet Invest"},{"key":"10.1111\/ced.12293-BIB0008|ced12293-cit-0008","doi-asserted-by":"crossref","first-page":"925","DOI":"10.1093\/hmg\/ddg097","article-title":"Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome","volume":"12","author":"Jobard","year":"2003","journal-title":"Hum Mol Genet"},{"key":"10.1111\/ced.12293-BIB0009|ced12293-cit-0009","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1086\/376609","article-title":"Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome","volume":"73","author":"Siegel","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1111\/ced.12293-BIB0010|ced12293-cit-0010","unstructured":"Leiden Open Variation Database. Mendelian Genes. Fermitin family homolog 1 https:\/\/grenada.lumc.nl\/LOVD2\/mendelian_genes\/variants.php?action=n=search_unique&select_db=FERMT1"}],"container-title":["Clinical and Experimental Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fced.12293","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/ced.12293\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,7,11]],"date-time":"2023-07-11T07:37:00Z","timestamp":1689061020000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/ced\/article\/39\/3\/340\/6621236"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,3,18]]},"references-count":10,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2014,4]]}},"URL":"https:\/\/doi.org\/10.1111\/ced.12293","relation":{},"ISSN":["0307-6938"],"issn-type":[{"value":"0307-6938","type":"print"}],"subject":[],"published":{"date-parts":[[2014,3,18]]}}}