📣 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.

Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy. (2016)

First Author: Fuller HR

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2016.06.004

PubMed Identifier: 27460344

Publication URI: http://europepmc.org/abstract/MED/27460344

Type: Journal Article/Review

Volume: 26

Parent Publication: Neuromuscular disorders : NMD

Issue: 9

ISSN: 0960-8966