| Literature DB >> 28395795 |
Salvador Martí1, Marian León2, Carmen Orellana3, Javier Prieto2, Xavier Ponsoda2, Carlos López-García2, Juan Jesús Vílchez4, Teresa Sevilla4, Josema Torres5.
Abstract
Human CMT2-FiPS4F1 cell line was generated from fibroblasts of a patient with Charcot-Marie-Tooth disease harbouring the following mutations in the GDAP1 gene in heterozygosis: p.Q163X/p.T288NfsX3. This patient did not present mutations in the PM22, MPZ or GJB genes. Human reprogramming factors OCT3/4, KLF4, SOX2 and C-MYC were delivered using a non-integrative methodology that involves the use of Sendai virus.Entities:
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Year: 2016 PMID: 28395795 DOI: 10.1016/j.scr.2016.11.017
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020