📣 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.

Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization. (2023)

First Author: Scarrott JM

Attributed to: Gene Therapy Innovation and Manufacturing Centre (GTIMC) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcac335

PubMed Identifier: 36632189

Publication URI: http://europepmc.org/abstract/MED/36632189

Type: Journal Article/Review

Volume: 5

Parent Publication: Brain communications

Issue: 1

ISSN: 2632-1297