📣 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.

The Parkinson's disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human. (2018)

First Author: Mir R

Attributed to: Understanding Signalling Pathways Mutated in Inherited Disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1042/bcj20180248

PubMed Identifier: 29743203

Publication URI: http://europepmc.org/abstract/MED/29743203

Type: Journal Article/Review

Volume: 475

Parent Publication: The Biochemical journal

Issue: 11

ISSN: 0264-6021