📣 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.

MFN2 deletion of exons 7 and 8: founder mutation in the UK population. (2015)

First Author: Carr AS

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

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/jns.12117

PubMed Identifier: 26114802

Publication URI: http://europepmc.org/abstract/MED/26114802

Type: Journal Article/Review

Volume: 20

Parent Publication: Journal of the peripheral nervous system : JPNS

Issue: 2

ISSN: 1085-9489