Mice with endogenous TDP -43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis (2018)

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

Parent Publication: The EMBO Journal

Issue: 11

ISSN: 0261-4189