📣 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.

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2. (2015)

First Author: Rossor AM

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awu356

PubMed Identifier: 25497877

Publication URI: http://europepmc.org/abstract/MED/25497877

Type: Journal Article/Review

Volume: 138

Parent Publication: Brain : a journal of neurology

Issue: Pt 2

ISSN: 0006-8950