Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene

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.

Bibliographic Details
Main Authors: Dunja Lukovic, Aranzazu Bolinches Amoros, Ana Artero Castro, Beatriz Pascual, Miguel Carballo, Imma Hernán, Slaven Erceg
Format: Article
Language:English
Published: Elsevier 2017-05-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506117300466