Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation. (2017)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41598-017-12396-2
PubMed Identifier: 28951556
Publication URI: http://europepmc.org/abstract/MED/28951556
Type: Journal Article/Review
Volume: 7
Parent Publication: Scientific reports
Issue: 1
ISSN: 2045-2322