{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,21]],"date-time":"2023-10-21T12:09:28Z","timestamp":1697890168758},"reference-count":4,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[1980,11,1]],"date-time":"1980-11-01T00:00:00Z","timestamp":341884800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Arch Dermatol Res"],"published-print":{"date-parts":[[1980,11]]},"DOI":"10.1007\/bf00406542","type":"journal-article","created":{"date-parts":[[2004,11,9]],"date-time":"2004-11-09T10:45:18Z","timestamp":1099997118000},"page":"209-210","source":"Crossref","is-referenced-by-count":17,"title":["HLA and porphyria cutanea tarda"],"prefix":"10.1007","volume":"269","author":[{"given":"L.","family":"Llorente","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Enr\ufffdquez","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Campillo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M. L.","family":"Pe\ufffda","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"1089","DOI":"10.1172\/JCI108560","volume":"58","author":"JP Kushner","year":"1976","unstructured":"Kushner JP, Barbuto AJ, Lee GR (1976) An inherited enzymatic defect in porphyria cutanea tarda: Decreased uroporphyrinogen decarboxylase activity. J Clin Invest 58:1089?1097","journal-title":"J Clin Invest"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"858","DOI":"10.1056\/NEJM197802162980702","volume":"298","author":"AV Benedetto","year":"1978","unstructured":"Benedetto AV, Kushner JP, Taylor JS (1978) Porphyria cutanea tarda in three generations of a single family. N Engl J Med 298:858?862","journal-title":"N Engl J Med"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1007\/BF00295407","volume":"44","author":"H Verneuil De","year":"1978","unstructured":"De Verneuil H, Aitken G, Nordmann Y (1978) Familial and sporadic porphyria cutanea: Two different diseases. Hum Genet 44:145?151","journal-title":"Hum Genet"},{"key":"CR4","first-page":"1","volume":"59","author":"GH Elder","year":"1980","unstructured":"Elder GH, Sheppard DM, Enr\u00edquez de Salamanca R, Olmos A (1980) Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase. Clin Sci Mol Med 59:1?8","journal-title":"Clin Sci Mol Med"}],"container-title":["Archives of Dermatological Research"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00406542.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00406542\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00406542","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,4]],"date-time":"2019-04-04T00:11:33Z","timestamp":1554336693000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00406542"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1980,11]]},"references-count":4,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1980,11]]}},"alternative-id":["BF00406542"],"URL":"https:\/\/doi.org\/10.1007\/bf00406542","relation":{},"ISSN":["0340-3696","1432-069X"],"issn-type":[{"value":"0340-3696","type":"print"},{"value":"1432-069X","type":"electronic"}],"subject":[],"published":{"date-parts":[[1980,11]]}}}