Human artificial chromosome-mediated genetic correction of human dystrophic skeletal muscle progenitors for the autologous cell therapy of Duchenne muscular dystrophy (2015)

First Author: Benedetti S.

Attributed to: Engineering human artificial chromosomes containing the dystrophin locus for autologous cell therapy of Duchenne Muscular Dystrophy. funded by MRC

No abstract provided

Type: Conference/Paper/Proceeding/Abstract

Volume: 26

Parent Publication: HUMAN GENE THERAPY

Issue: 10

ISSN: 1043-0342