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Challenges in cell transplantation for muscular dystrophy. (2021)

First Author: Galli F

Attributed to: Cell mediated gene therapy for Duchenne muscular dystrophy: trans-correction of resident nuclei to amplify dystrophin expression funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.yexcr.2021.112908

PubMed Identifier: 34736920

Publication URI: http://europepmc.org/abstract/MED/34736920

Type: Journal Article/Review

Volume: 409

Parent Publication: Experimental cell research

Issue: 1

ISSN: 0014-4827