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dc.contributor.authorXue Zhang
dc.contributor.authorZilong Li
dc.contributor.authorYi Liu
dc.contributor.authorHongmei Xin
dc.contributor.authorZhongtao Gai
dc.contributor.otherChildren’s Hospital Affiliated to Shandong University, Jinan, Shandong 250022, China; The Second Hospital of Shandong University, Jinan, Shandong 250033, China
dc.contributor.otherChildren’s Hospital Affiliated to Shandong University, Jinan, Shandong 250022, China
dc.contributor.otherChildren’s Hospital Affiliated to Shandong University, Jinan, Shandong 250022, China
dc.contributor.otherChildren’s Hospital Affiliated to Shandong University, Jinan, Shandong 250022, China; Corresponding authors.
dc.contributor.otherChildren’s Hospital Affiliated to Shandong University, Jinan, Shandong 250022, China; Corresponding authors.
dc.date.accessioned2024-03-17T07:53:16Z
dc.date.accessioned2025-10-08T09:19:55Z
dc.date.available2025-10-08T09:19:55Z
dc.date.issued01-06-2024
dc.identifier.urihttp://digilib.fisipol.ugm.ac.id/repo/handle/15717717/39962
dc.description.abstractSegawa syndrome, an autosomal recessive genetic disorder, arises from homozygous or compound heterozygous mutations in the TH gene. We established an induced pluripotent stem cell (iPSC) line from peripheral blood mononuclear cells (PBMCs) of an 4-month-old girl with Segawa syndrome, who carried compound heterozygous mutations of c.739G > A/chr11:2188714 and c.1471G > C/chr11:2185579 in TH. The iPSCs displayed a normal karyotype, expressed pluripotency markers, were devoid of genomically integrated episomal plasmids, and demonstrated trilineage differentiation potential in vitro.
dc.language.isoEN
dc.publisherElsevier
dc.subject.lccBiology (General)
dc.titleEstablishment of a non-integrated iPSC (SDQLCHi066-A) line derived from Segawa syndrome patients harboring heterozygous mutations in the TH gene (p.G247S and p.D491H)
dc.typeArticle
dc.description.doi10.1016/j.scr.2024.103392
dc.title.journalStem Cell Research
dc.identifier.oaioai:doaj.org/journal:ef9136ed7f31416788ef31c39bec46ba


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