| Literature DB >> 30312873 |
Caroline Amalie Brunbjerg Hey1, Katarina Beata Saltõkowa1, Lasse Jonsgaard Larsen1, Zeynep Tümer1, Karen Brøndum-Nielsen1, Karen Grønskov1, Tina Duelund Hjortshøj1, Lisbeth Birk Møller2.
Abstract
Bardet-Biedl syndrome (BBS) is genetically heterogeneous with at least 21 genes involved, and BBS10 encodes, together with BBS6 and BBS12, chaperonin-like proteins which are important for the assembly of the multiprotein complex, the BBSome encoded by other BBS genes. Here we describe the successful generation of an induced pluripotent stem cell (iPSC) line KCi002-A from a male with BBS, homozygous for the disease causing variant c.271insT, p.(Cys91fsX95) in BBS10. Resource table.Entities:
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Year: 2018 PMID: 30312873 DOI: 10.1016/j.scr.2018.09.013
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020