📣 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.

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)

First Author: Ababneh NA

Attributed to: Computational Genomics Analysis and Training programme (CGAT) 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