📣 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.

Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT. (2017)

First Author: Tomaselli PJ

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000003819

PubMed Identifier: 28283593

Publication URI: http://europepmc.org/abstract/MED/28283593

Type: Journal Article/Review

Volume: 88

Parent Publication: Neurology

Issue: 15

ISSN: 0028-3878