📣 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.

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy. (2016)

First Author: Zaharieva IT

Attributed to: Periodic paralysis: from molecules to mice funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awv352

PubMed Identifier: 26700687

Publication URI: http://europepmc.org/abstract/MED/26700687

Type: Journal Article/Review

Volume: 139

Parent Publication: Brain : a journal of neurology

Issue: Pt 3

ISSN: 0006-8950