Myopathy-inducing mutation H40Y in ACTA1 hampers actin filament structure and function. (2016)

First Author: Chan C
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/10.1016/j.bbadis.2016.04.013

PubMed Identifier: 27112274

Publication URI: http://europepmc.org/abstract/MED/27112274

Type: Journal Article/Review

Volume: 1862

Parent Publication: Biochimica et biophysica acta

Issue: 8

ISSN: 0006-3002