Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction. (2018)

First Author: Jungbluth H
Attributed to:  Determining how mutations in actin lead to skeletal muscle weakness funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/nrneurol.2017.191

PubMed Identifier: 29391587

Publication URI: http://europepmc.org/abstract/MED/29391587

Type: Journal Article/Review

Volume: 14

Parent Publication: Nature reviews. Neurology

Issue: 3

ISSN: 1759-4758