📣 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.

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses. (2024)

First Author: Gustavsson EK

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/10.1016/s1474-4422(24)00121-2

PubMed Identifier: 38614108

Publication URI: http://europepmc.org/abstract/MED/38614108

Type: Journal Article/Review

Volume: 23

Parent Publication: The Lancet. Neurology

Issue: 6

ISSN: 1474-4422