Generation of two genomic-integration-free DMD iPSC lines with mutations affecting all dystrophin isoforms and potentially amenable to exon-skipping. (2020)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.scr.2019.101688
PubMed Identifier: 32087527
Publication URI: http://europepmc.org/abstract/MED/32087527
Type: Journal Article/Review
Volume: 43
Parent Publication: Stem cell research
ISSN: 1873-5061