{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T14:04:06Z","timestamp":1761746646998,"version":"build-2065373602"},"reference-count":5,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2021,7,1]],"date-time":"2021-07-01T00:00:00Z","timestamp":1625097600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,7,1]],"date-time":"2021-07-01T00:00:00Z","timestamp":1625097600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,5,21]],"date-time":"2021-05-21T00:00:00Z","timestamp":1621555200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["R01DC005575","R01DC012115"],"award-info":[{"award-number":["R01DC005575","R01DC012115"]}],"id":[{"id":"10.13039\/100000002","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":[[2021,7]]},"DOI":"10.1016\/j.scr.2021.102405","type":"journal-article","created":{"date-parts":[[2021,5,24]],"date-time":"2021-05-24T12:38:13Z","timestamp":1621859893000},"page":"102405","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"special_numbering":"C","title":["Derivation of iPSC line UMi029-A bearing a hearing-loss associated variant in the SMPX gene"],"prefix":"10.1016","volume":"54","author":[{"given":"Derek M.","family":"Dykxhoorn","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiaoying","family":"Tong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicholas C.","family":"Gosstola","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xue Zhong","family":"Liu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.scr.2021.102405_b0005","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1016\/j.ijporl.2017.10.040","article-title":"A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss","volume":"104","author":"Niu","year":"2018","journal-title":"Int. J. Pediatr. Otorhinolaryngol."},{"issue":"5","key":"10.1016\/j.scr.2021.102405_b0010","doi-asserted-by":"crossref","first-page":"327","DOI":"10.2174\/1389202919666171218163046","article-title":"X-linked sensorineural hearing loss: a literature review","volume":"19","author":"Corvino","year":"2018","journal-title":"Curr. Genomics"},{"key":"10.1016\/j.scr.2021.102405_b0015","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1016\/j.ijporl.2018.07.022","article-title":"Skewed X-chromosome inactivation and next-generation sequencing to identify a novel SMPX variants associated with X-linked hearing loss in a Chinese family","volume":"113","author":"Gao","year":"2018","journal-title":"Int. J. Pediatr. Otorhinolaryngol."},{"issue":"6","key":"10.1016\/j.scr.2021.102405_b0020","doi-asserted-by":"crossref","first-page":"723","DOI":"10.1038\/s10038-018-0443-x","article-title":"A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family","volume":"63","author":"Deng","year":"2018","journal-title":"J. Hum. Genet."},{"issue":"11","key":"10.1016\/j.scr.2021.102405_b0025","doi-asserted-by":"crossref","DOI":"10.1002\/mgg3.967","article-title":"Whole-exome sequencing identifies a donor splice-site variant in SMPX that causes rare X-linked congenital deafness","volume":"7","author":"Lv","year":"2019","journal-title":"Mol. Genet. Genomic Med."}],"container-title":["Stem Cell Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1873506121002518?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1873506121002518?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T11:34:59Z","timestamp":1761737699000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1873506121002518"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,7]]},"references-count":5,"alternative-id":["S1873506121002518"],"URL":"https:\/\/doi.org\/10.1016\/j.scr.2021.102405","relation":{},"ISSN":["1873-5061"],"issn-type":[{"type":"print","value":"1873-5061"}],"subject":[],"published":{"date-parts":[[2021,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Derivation of iPSC line UMi029-A bearing a hearing-loss associated variant in the SMPX gene","name":"articletitle","label":"Article Title"},{"value":"Stem Cell Research","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.scr.2021.102405","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2021 Published by Elsevier B.V.","name":"copyright","label":"Copyright"}],"article-number":"102405"}}