{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T20:11:53Z","timestamp":1791231113276,"version":"4.1.0"},"reference-count":9,"publisher":"Oxford University Press (OUP)","issue":"8","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":49,"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":[[2015,12]]},"DOI":"10.1111\/ced.12702","type":"journal-article","created":{"date-parts":[[2015,7,14]],"date-time":"2015-07-14T19:41:57Z","timestamp":1436902917000},"page":"860-864","source":"Crossref","is-referenced-by-count":17,"title":["Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in<i>KITLG<\/i>"],"prefix":"10.1093","volume":"40","author":[{"given":"A.","family":"Cuell","sequence":"first","affiliation":[{"name":"Department of Dermatology; Birmingham Children's Hospital; NHS Foundation Trust; Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N.","family":"Bansal","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Solihull Hospital; Heart of England NHS Foundation Trust; Solihull UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T.","family":"Cole","sequence":"additional","affiliation":[{"name":"Department of Clinical Genetics; Birmingham Women's Hospital; NHS Foundation Trust; Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. R.","family":"Kaur","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Solihull Hospital; Heart of England NHS Foundation Trust; Solihull UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.","family":"Lee","sequence":"additional","affiliation":[{"name":"Genetic Skin Disease Group; St John's Institute of Dermatology; King's College London; London UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A.","family":"Loffeld","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Solihull Hospital; Heart of England NHS Foundation Trust; Solihull UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C.","family":"Moss","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Birmingham Children's Hospital; NHS Foundation Trust; Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"O'Donnell","sequence":"additional","affiliation":[{"name":"Department of Clinical Genetics; Birmingham Women's Hospital; NHS Foundation Trust; Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T.","family":"Takeichi","sequence":"additional","affiliation":[{"name":"Genetic Skin Disease Group; St John's Institute of Dermatology; King's College London; London UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C. K.","family":"Thind","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Birmingham Children's Hospital; NHS Foundation Trust; Birmingham UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. A.","family":"McGrath","sequence":"additional","affiliation":[{"name":"Genetic Skin Disease Group; St John's Institute of Dermatology; King's College London; London UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2015,7,14]]},"reference":[{"key":"10.1111\/ced.12702-BIB0001|ced12702-cit-0001","doi-asserted-by":"crossref","first-page":"931","DOI":"10.1001\/archderm.1978.01640180065016","article-title":"Hereditary congenital hypopigmented and hyperpigmented macules","volume":"114","author":"Westerhof","year":"1978","journal-title":"Arch Dermatol"},{"key":"10.1111\/ced.12702-BIB0002|ced12702-cit-0002","doi-asserted-by":"crossref","first-page":"1234","DOI":"10.1038\/jid.2011.29","article-title":"KITLG mutations cause familial progressive hyper- and hypopigmentation","volume":"131","author":"Amyere","year":"2011","journal-title":"J Invest Dermatol"},{"key":"10.1111\/ced.12702-BIB0003|ced12702-cit-0003","doi-asserted-by":"crossref","first-page":"672","DOI":"10.1016\/j.ajhg.2009.03.019","article-title":"Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation","volume":"84","author":"Wang","year":"2009","journal-title":"Am J Hum Genet"},{"key":"10.1111\/ced.12702-BIB0004|ced12702-cit-0004","doi-asserted-by":"crossref","first-page":"2221","DOI":"10.1038\/jid.2013.145","article-title":"Mutations in ABCB6 cause\u00a0dyschromatosis universalis hereditaria","volume":"133","author":"Zhang","year":"2013","journal-title":"J Invest Dermatol"},{"key":"10.1111\/ced.12702-BIB0005|ced12702-cit-0005","doi-asserted-by":"crossref","first-page":"1182","DOI":"10.1038\/jid.2011.67","article-title":"The genetic determination of skin pigmentation: KITLG and the KITLG\/c-Kit pathway as key players in the onset of human\u00a0familial\u00a0pigmentary diseases","volume":"131","author":"Picardo","year":"2011","journal-title":"J Invest Dermatol"},{"key":"10.1111\/ced.12702-BIB0006|ced12702-cit-0006","doi-asserted-by":"crossref","first-page":"1111","DOI":"10.1111\/bjd.13413","article-title":"Progressive hyperpigmentation in a Taiwanese child due to an inborn error of vitamin B12 metabolism (cblJ)","volume":"172","author":"Takeichi","year":"2014","journal-title":"Br J Dermatol"},{"key":"10.1111\/ced.12702-BIB0007|ced12702-cit-0007","doi-asserted-by":"crossref","first-page":"96","DOI":"10.3315\/jdcr.2012.1111","article-title":"Dyschromatosis universalis hereditaria: an infrequently occurring entity in Europe","volume":"6","author":"Merino de Paz","year":"2012","journal-title":"J Dermatol Case Rep"},{"key":"10.1111\/ced.12702-BIB0008|ced12702-cit-0008","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1002\/ajmg.a.20519","article-title":"Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation","volume":"125A","author":"Nuber","year":"2004","journal-title":"Am J Med Genet A"},{"key":"10.1111\/ced.12702-BIB0009|ced12702-cit-0009","unstructured":"Catalogue of Somatic Mutations in Cancer (COSMIC) database http:\/\/cancer.sanger.ac.uk\/cosmic\/gene\/analysis?ln=KITLG#histo"}],"container-title":["Clinical and Experimental Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fced.12702","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/ced.12702\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,2,14]],"date-time":"2023-02-14T14:41:52Z","timestamp":1676385712000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/ced\/article\/40\/8\/860\/6621481"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,7,14]]},"references-count":9,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2015,12]]}},"URL":"https:\/\/doi.org\/10.1111\/ced.12702","archive":["Portico"],"relation":{},"ISSN":["0307-6938"],"issn-type":[{"value":"0307-6938","type":"print"}],"subject":[],"published":{"date-parts":[[2015,7,14]]}}}