{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T14:06:22Z","timestamp":1761746782815,"version":"build-2065373602"},"reference-count":4,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2024,3,1]],"date-time":"2024-03-01T00:00:00Z","timestamp":1709251200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,3,1]],"date-time":"2024-03-01T00:00:00Z","timestamp":1709251200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,1,22]],"date-time":"2024-01-22T00:00:00Z","timestamp":1705881600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100009592","name":"Beijing Municipal Science and Technology Commission, Adminitrative Commission of Zhongguancun Science Park","doi-asserted-by":"publisher","award":["Z211100002921005"],"award-info":[{"award-number":["Z211100002921005"]}],"id":[{"id":"10.13039\/501100009592","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Stem Cell Research"],"published-print":{"date-parts":[[2024,3]]},"DOI":"10.1016\/j.scr.2024.103318","type":"journal-article","created":{"date-parts":[[2024,1,23]],"date-time":"2024-01-23T13:02:49Z","timestamp":1706014969000},"page":"103318","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"special_numbering":"C","title":["Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome"],"prefix":"10.1016","volume":"75","author":[{"given":"Yi-bo","family":"Wang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ya-feng","family":"Lv","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5430-1608","authenticated-orcid":false,"given":"Ye","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wei","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.scr.2024.103318_b0005","unstructured":"Xiaohui, D., Wei, W., Mingrui, D., Lu, W., Ziqiang, S., Zhaoxia, W., et al., 2019. 'Clinical and genetic analysis of a patient with Perrault syndrome and additional neurological features', Chin. J. Med. Genet., June 2019\uff0cV01. 36\uff0cNo. 6."},{"key":"10.1016\/j.scr.2024.103318_b0010","doi-asserted-by":"crossref","first-page":"974","DOI":"10.1007\/s00415-011-6285-5","article-title":"Perrault syndrome: further evidence for genetic heterogeneity","volume":"259","author":"Jenkinson","year":"2012","journal-title":"J. Neurol."},{"key":"10.1016\/j.scr.2024.103318_b0015","doi-asserted-by":"crossref","DOI":"10.1016\/j.scr.2022.102945","article-title":"Production and characterization of human induced pluripotent stem cell line (PUMCi002-A) from a Krabbe patient related control to study disease mechanisms associated with GALC mutation","volume":"65","author":"Lv","year":"2022","journal-title":"Stem Cell Res."},{"key":"10.1016\/j.scr.2024.103318_b0020","doi-asserted-by":"crossref","first-page":"282","DOI":"10.1016\/j.ajhg.2010.07.007","article-title":"Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome","volume":"87","author":"Pierce","year":"2010","journal-title":"Am. J. Hum. Genet."}],"container-title":["Stem Cell Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1873506124000163?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1873506124000163?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T11:38:33Z","timestamp":1761737913000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1873506124000163"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,3]]},"references-count":4,"alternative-id":["S1873506124000163"],"URL":"https:\/\/doi.org\/10.1016\/j.scr.2024.103318","relation":{},"ISSN":["1873-5061"],"issn-type":[{"type":"print","value":"1873-5061"}],"subject":[],"published":{"date-parts":[[2024,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome","name":"articletitle","label":"Article Title"},{"value":"Stem Cell Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.scr.2024.103318","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 The Authors. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}],"article-number":"103318"}}