📣 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 C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder. (2013)

First Author: Smith BN

Attributed to: RNA processing proteins and neurodegeneration: exploring mechanisms and modelling disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2012.98

PubMed Identifier: 22692064

Publication URI: http://europepmc.org/abstract/MED/22692064

Type: Journal Article/Review

Volume: 21

Parent Publication: European journal of human genetics : EJHG

Issue: 1

ISSN: 1018-4813