Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repair. (2020)
Attributed to:
Identifying effectors of mutant C9Orf72 ALS/FTD to combat neurodegeneration
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddaa106
PubMed Identifier: 32504093
Publication URI: http://europepmc.org/abstract/MED/32504093
Type: Journal Article/Review
Volume: 29
Parent Publication: Human molecular genetics
Issue: 13
ISSN: 0964-6906