Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene
Summary
A human iPSC line, IISHDOi004-A, from fibroblasts obtained from a patient with Usher syndrome, harboring a homozygous mutation in the USH2A gene (c.2276G>T; p.Cys759Phe) has been generated. Reprogramming factors Oct3/4, Sox2, Klf4, and c-Myc were delivered using Sendai virus. Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.
Authors | Zurita-Díaz F, Ortuño-Costela MDC, Moreno-Izquierdo A, Galbis L, Millán JM, Ayuso C, Garesse R, Gallardo ME |
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Journal | Stem cell research |
Publication Date | 2018 Aug;31:152-156 |
PubMed | 30096711 |
DOI | 10.1016/j.scr.2018.08.002 |