Generation of induced pluripotent stem cells, KCi002-A derived from a patient with Bardet-Biedl syndrome homozygous for the BBS10 variant c.271insT

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

  • Caroline Amalie Brunbjerg Hey
  • Katarina Beata Saltõkowa
  • Lasse Jonsgaard Larsen
  • Tümer, Zeynep
  • Karen Brøndum-Nielsen
  • Karen Grønskov
  • Tina Duelund Hjortshøj
  • Lisbeth Birk Møller

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.

OriginalsprogEngelsk
TidsskriftStem Cell Research
Vol/bind33
Sider (fra-til)46-50
ISSN1873-5061
DOI
StatusUdgivet - 2018

Bibliografisk note

Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.

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