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

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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… Click to show full abstract

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.

Keywords: caused mutation; line; patient retinitis; retinitis pigmentosa; pigmentosa caused; human ipsc

Journal Title: Stem cell research
Year Published: 2017

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