Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene
Summary
The human iPSC cell line, RP2-FiPS4F1 (RCPFi001-A), derived from dermal fibroblasts from the patient with retinitis pigmentosa caused by the mutation of the gene PRPF8, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 reprogramming factors. Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.
Authors | Lukovic D, Bolinches-Amorós A, Artero-Castro A, Pascual B, Carballo M, Hernan I, Erceg S |
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Journal | Stem cell research |
Publication Date | 2017 May;21:23-25 |
PubMed | 28677533 |
DOI | 10.1016/j.scr.2017.03.007 |