{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,16]],"date-time":"2023-09-16T11:10:39Z","timestamp":1694862639694},"reference-count":5,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[1996,3,1]],"date-time":"1996-03-01T00:00:00Z","timestamp":825638400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[1996,3]]},"DOI":"10.1007\/bf01799405","type":"journal-article","created":{"date-parts":[[2005,6,21]],"date-time":"2005-06-21T16:34:14Z","timestamp":1119371654000},"page":"109-111","source":"Crossref","is-referenced-by-count":8,"title":["Pernicious anaemia and hypoparathyroidism in a patient with Kearns\u2010Sayre syndrome with mitochondrial DNA duplication"],"prefix":"10.1002","volume":"19","author":[{"given":"M. J.","family":"Abramowicz","sequence":"first","affiliation":[{"name":"Departments of Genetics and Pediatrics Brussels University Clincs, Erasme Hospital and Huderf  Brussels Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Cochaux","sequence":"additional","affiliation":[{"name":"Departments of Genetics and Pediatrics Brussels University Clincs, Erasme Hospital and Huderf  Brussels Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L. H. F.","family":"Cohen","sequence":"additional","affiliation":[{"name":"Departments of Genetics and Pediatrics Brussels University Clincs, Erasme Hospital and Huderf  Brussels Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Vamos","sequence":"additional","affiliation":[{"name":"Departments of Genetics and Pediatrics Brussels University Clincs, Erasme Hospital and Huderf  Brussels Belgium"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[1996,3]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1038\/ng0994-83"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410030611"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/ng1294-313"},{"key":"e_1_2_1_5_1","first-page":"364","article-title":"Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia","volume":"50","author":"R\u00f6tig A","year":"1992","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_6_1","first-page":"1","volume-title":"Mitochondrial DNA in Human Pathology","author":"Schon EA","year":"1993"}],"container-title":["Journal of Inherited Metabolic Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/BF01799405","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/BF01799405","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,15]],"date-time":"2023-09-15T13:10:18Z","timestamp":1694783418000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1007\/BF01799405"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,3]]},"references-count":5,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1996,3]]}},"alternative-id":["10.1007\/BF01799405"],"URL":"https:\/\/doi.org\/10.1007\/bf01799405","archive":["Portico"],"relation":{},"ISSN":["0141-8955","1573-2665"],"issn-type":[{"value":"0141-8955","type":"print"},{"value":"1573-2665","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,3]]}}}