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

First Author: Zaharieva IT
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

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