📣 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.

Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation (2015)

First Author: Kiely A

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13024-015-0038-3

PubMed Identifier: 26306801

Publication URI: http://europepmc.org/abstract/MED/26306801

Type: Journal Article/Review

Parent Publication: Molecular Neurodegeneration

Issue: 1

ISSN: 1750-1326