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Generation of a human iPSC line from a patient with a defect of intergenomic communication
Francisco Zurita1, Teresa Galera1, Cristina González-Páramos1
1Departamento de Bioquímica, Instituto de Investigaciones Biomédicas "Alberto Sols ", Facultad de Medicina (UAM-CSIC), Spain; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Madrid, Spain; Instituto de Investigación Hospital 12 de Octubre ("i + 12"), Madrid, Spain.
Abstract:
Human iPSC line PG64SV.2 was generated from fibroblasts of a patient with a defect of intergenomic communication. This patient harbored a homozygous mutation (c.2243G>C; p.Trp748Ser) in the gene encoding the catalytic subunit of the mitochondrial DNA polymerase gamma gene (POLG). Reprogramming factors Oct3/4, Sox2, Klf4, and cMyc were delivered using a non integrative methodology that involves the use of Sendai virus.
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