📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Repair or replace? Exploiting novel gene and cell therapy strategies for muscular dystrophies. (2013)

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

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/febs.12178

PubMed Identifier: 23387802

Publication URI: http://europepmc.org/abstract/MED/23387802

Type: Journal Article/Review

Volume: 280

Parent Publication: The FEBS journal

Issue: 17

ISSN: 1742-464X