Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. (2018)
Attributed to:
New humanised mouse models for dissecting the pathobiology of disease, using FUS-ALS as a paradigm
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.15252/embj.201798684
PubMed Identifier: 29764981
Publication URI: http://europepmc.org/abstract/MED/29764981
Type: Journal Article/Review
Volume: 37
Parent Publication: The EMBO journal
Issue: 11
ISSN: 0261-4189