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To derive Duchenne muscular dystrophy patient specific induced pluripotent stem cells (iPSCs) from CD3 + T cells of DMD patients using episomal reprogramming and characterization of these DMD-iPSCs using immunofluorescence to confirm their pluripotent state.

Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3+ T cells towards induced pluripotent stem cells