📣 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.

PLP1 mutations and central demyelination: Evidence from electrophysiologic phenotyping in female manifesting carriers. (2017)

First Author: Keogh MJ

Attributed to: Examining the coupling of small GTPase activation and metabolism of the phosphoinositide lipid PI(3,5)P2 in Charcot Marie Tooth Type 4 Neuropathies funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/cpj.0000000000000346

PubMed Identifier: 29620084

Publication URI: http://europepmc.org/abstract/MED/29620084

Type: Journal Article/Review

Volume: 7

Parent Publication: Neurology. Clinical practice

Issue: 5

ISSN: 2163-0402